{
  "title": "Recall Radar normalized recalls",
  "generated_at_utc": "2026-09-07T22:36:03.503Z",
  "source": "openFDA enforcement APIs",
  "record_count": 36,
  "records": [
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-24",
      "recall_number": "D-0831-2026",
      "event_id": "99711",
      "recalling_firm": "Hikma Pharmaceuticals USA INC.",
      "product_description": "Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05) bottles, Rx only, Manufactured for: Exelan Pharmaceuticals, Inc., Boca Raton, FL 33432, Manufactured by: West-Ward Columbus Inc., Columbus, OH 43228.",
      "reason_for_recall": "Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "a) 25,970 bottles; b) 2,384 bottles",
      "code_info": "a) Lot #: AC5470A, Exp. Date July 2027 b) Lot #: AC5470B, Exp. Date July 2027",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0831-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-18",
      "recall_number": "H-1264-2026",
      "event_id": "99716",
      "recalling_firm": "Dreyer's Grand Ice Cream Inc.",
      "product_description": "Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.",
      "reason_for_recall": "Foreign object: products may contain glass pieces",
      "distribution_pattern": "The adulterated product was distributed to the following States: AL, AR, AZ, CA,CO,CT, FL,GA, IA,ID, IL, KS, LA, MA,MD,MI, MN,MO, NC, ND, NH, NJ, NV, NY, OH, PA, PR, TN TX, UT, VA, VI, WA, and WI.",
      "product_quantity": "644 pallets",
      "code_info": "Batch code/ Best Before (bottom of package): LLA616903 30 SEP 2027 LLA617003 30 SEP 2027 LLA617103 30 SEP 2027 LLA617203 30 SEP 2027 LLA617303 30 SEP 2027 LLA617403 30 SEP 2027 LLA617503 30 SEP 2027 LLA617603 30 SEP 2027 LLA620303 31 OCT 2027 LLA620403 31 OCT 2027 LLA620503 31 OCT 2027 LLA620603 31 OCT 2027 LLA620703 31 OCT 2027 LLA620803 31 OCT 2027 LLA620903 31 OCT 2027 LLA621003 31 OCT 2027 LLA621103 31 OCT 2027 LLA621203 31 OCT 2027 LLA621303 30 NOV 2027 LLA621403 30 NOV 2027 LLA621503 30 NOV 2027 LLA621603 30 NOV 2027",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1264-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-18",
      "recall_number": "H-1265-2026",
      "event_id": "99716",
      "recalling_firm": "Dreyer's Grand Ice Cream Inc.",
      "product_description": "Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.",
      "reason_for_recall": "Foreign object: products may contain glass pieces",
      "distribution_pattern": "The adulterated product was distributed to the following States: AL, AR, AZ, CA,CO,CT, FL,GA, IA,ID, IL, KS, LA, MA,MD,MI, MN,MO, NC, ND, NH, NJ, NV, NY, OH, PA, PR, TN TX, UT, VA, VI, WA, and WI.",
      "product_quantity": "685 pallets",
      "code_info": "Batch code/ Best Before (bottom of package): LLA617603 30 JUN 2027 LLA617703 30 JUN 2027 LLA617803 30 JUN 2027 LLA617903 30 JUN 2027 LLA618003 30 JUN 2027 LLA618103 30 JUN 2027 LLA618203 31 JUL 2027 LLA618303 31 JUL 2027 LLA618403 31 JUL 2027 LLA618503 31 JUL 2027 LLA619003 31 JUL 2027 LLA619103 31 JUL 2027 LLA619203 31 JUL 2027 LLA619303 31 JUL 2027 LLA619403 31 JUL 2027 LLA619503 31 JUL 2027",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1265-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-18",
      "recall_number": "H-1266-2026",
      "event_id": "99716",
      "recalling_firm": "Dreyer's Grand Ice Cream Inc.",
      "product_description": "Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.",
      "reason_for_recall": "Foreign object: products may contain glass pieces",
      "distribution_pattern": "The adulterated product was distributed to the following States: AL, AR, AZ, CA,CO,CT, FL,GA, IA,ID, IL, KS, LA, MA,MD,MI, MN,MO, NC, ND, NH, NJ, NV, NY, OH, PA, PR, TN TX, UT, VA, VI, WA, and WI.",
      "product_quantity": "281 pallets",
      "code_info": "Batch code/ Best Before (bottom of package): LLA616803 30 SEP 2027 LLA616903 30 SEP 2027 LLA619703 31 OCT 2027 UPC Bottom of package: 041548244044 LLA619803 31 OCT 2027 LLA619903 31 OCT 2027 LLA620003 31 OCT 2027 LLA620103 31 OCT 2027 LLA620203 31 OCT 2027 LLA620303 31 OCT 2027",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1266-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-18",
      "recall_number": "H-1268-2026",
      "event_id": "99716",
      "recalling_firm": "Dreyer's Grand Ice Cream Inc.",
      "product_description": "Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.",
      "reason_for_recall": "Foreign object: products may contain glass pieces",
      "distribution_pattern": "The adulterated product was distributed to the following States: AL, AR, AZ, CA,CO,CT, FL,GA, IA,ID, IL, KS, LA, MA,MD,MI, MN,MO, NC, ND, NH, NJ, NV, NY, OH, PA, PR, TN TX, UT, VA, VI, WA, and WI.",
      "product_quantity": "226 pallets",
      "code_info": "Batch code/ Best Before (bottom of package): LLA618503 31 JUL 2027 LLA618603 31 JUL 2027 LLA618703 31 JUL 2027 LLA618803 31 JUL 2027 LLA618903 31 JUL 2027 LLA619003 31 JUL 2027",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1268-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-18",
      "recall_number": "Z-3035-2026",
      "event_id": "99607",
      "recalling_firm": "Olympus Corporation of the Americas",
      "product_description": "POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories",
      "reason_for_recall": "Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of Kansas and Florida. The countries of Australia, European Union, Japan.",
      "product_quantity": "335 units",
      "code_info": "Model Number: PS-0523CJDA. UDI-DI: 00821925044531. Lot Number: FR490902.",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3035-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-11",
      "recall_number": "H-1271-2026",
      "event_id": "99690",
      "recalling_firm": "CUISINE, KETTLE",
      "product_description": "Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14 OZ (397g), with UPC 1 94346474004. Must Keep Refrigerated.",
      "reason_for_recall": "Product had a presumptive positive test result for Listeria monocytogenes",
      "distribution_pattern": "The recalled product was distributed to the following States: IL, NV, NM, CA, OK, TX, PA, OH, NC, NY, GA, and AR.",
      "product_quantity": "540 cases",
      "code_info": "Best By/ Use By: 8/22/2026",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1271-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-11",
      "recall_number": "H-1278-2026",
      "event_id": "99629",
      "recalling_firm": "Byron White Formulas, Inc.",
      "product_description": "Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404",
      "reason_for_recall": "Label does not declare walnuts in English",
      "distribution_pattern": "Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.",
      "product_quantity": "10,403 units",
      "code_info": "Lot Code Format = MMD,DYY: 022,224. 061,424. 092,324. 022,125. 071,825. 112,125. 040,826.",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1278-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-10",
      "recall_number": "D-0790-2026",
      "event_id": "99604",
      "recalling_firm": "Church & Dwight Co., Inc.",
      "product_description": "Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, Distributed by Church & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205.",
      "reason_for_recall": "CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing",
      "distribution_pattern": "US Nationwide.",
      "product_quantity": "318,600 cartons",
      "code_info": "Lot # UN52882, Exp Date: 04/30/2028; Lot # UN53431, Exp Date: 06/30/2028; Lot # UN60411, Exp Date: 08/31/2028.",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0790-2026%22"
    },
    {
      "category": "Food",
      "classification": "Not Yet Classified",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-10",
      "recall_number": "N/A",
      "event_id": "99642",
      "recalling_firm": "Africando Foods LLC",
      "product_description": "Clear glass bottle with black screw lid with multi label which reads in part as \"***AFRICANDO FOODS, LLC ALFREDO HOT SAUCE, Net Weight 8 oz. ***INGREDIENTS: Habenaro Peppers, Garlic, Onions, Water, Distilled 5% White Vinegar, Spices***Manufactured and Packed By Africando Foods, LLC 1121S Gilbert Ct. Iowa City, IA 52240***\"",
      "reason_for_recall": "Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list",
      "distribution_pattern": "8 wholesale and retail locations in IA, KY and IL",
      "product_quantity": "N/A",
      "code_info": "UPC: 860004527114 AF25296, exp. 10/23/2026 AF25303, exp. 10/30/2026 AF25319, exp. 11/15/2026 AF25333, exp. 11/29/2026 AF25343, exp. 12/09/2026 AF25357, exp. 12/23/2026",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22N%2FA%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0775-2026",
      "event_id": "99584",
      "recalling_firm": "ACCORD HEALTHCARE, INC.",
      "product_description": "Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-447-17.",
      "reason_for_recall": "Subpotent Drug",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "N/A",
      "code_info": "Lot #: D2401927, D2401833, Exp. Date 08/31/2026; D2402551, D2402552, Exp. Date 11/30/2026; D2500220, Exp. Date 12/31/2026; D2500223, Exp. Date 01/31/2027.",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0775-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0776-2026",
      "event_id": "99584",
      "recalling_firm": "ACCORD HEALTHCARE, INC.",
      "product_description": "Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-448-17.",
      "reason_for_recall": "Subpotent Drug",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "N/A",
      "code_info": "Lot #: D2401834, D2401982, Exp. Date 08/31/2026; D2402584, D2402585, D2402586, D2402588, D2402587, D2402589, Exp Date. 11/30/2026.",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0776-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0777-2026",
      "event_id": "99584",
      "recalling_firm": "ACCORD HEALTHCARE, INC.",
      "product_description": "Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-449-17.",
      "reason_for_recall": "Subpotent Drug",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "N/A",
      "code_info": "Lot #: D2402016, D2402017, Exp. Date 08/31/2026",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0777-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0781-2026",
      "event_id": "99584",
      "recalling_firm": "ACCORD HEALTHCARE, INC.",
      "product_description": "Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-453-17.",
      "reason_for_recall": "Subpotent Drug",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "N/A",
      "code_info": "Lot #: D2401983, Exp. Date 08/31/2026; D2402640, D2402641, Exp. Date 11/30/2026; D2500224, Exp. Date 01/31/2027.",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0781-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0782-2026",
      "event_id": "99584",
      "recalling_firm": "ACCORD HEALTHCARE, INC.",
      "product_description": "Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg), packaged in a) 90-count bottles (NDC 16729-454-15) b) 1000-count bottles (NDC 16729-454-17), Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India.",
      "reason_for_recall": "Subpotent Drug",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "N/A",
      "code_info": "a) Lot # D2402125, D2402126, D2402127, Exp. Date 09/30/2026. b) Lot #: D2402523, D2402524, Exp. Date 11/30/2026.",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0782-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0783-2026",
      "event_id": "99584",
      "recalling_firm": "ACCORD HEALTHCARE, INC.",
      "product_description": "Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-455-17.",
      "reason_for_recall": "Subpotent Drug",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "N/A",
      "code_info": "Lot #: D2402195, D2402196, D2402197, Exp. Date 09/30/2026.",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0783-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0785-2026",
      "event_id": "99584",
      "recalling_firm": "ACCORD HEALTHCARE, INC.",
      "product_description": "Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg), packaged in a) 90-count bottles (NDC 16729-457-15) and b) 1000-count bottles (NDC 16729-457-17), Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India.",
      "reason_for_recall": "Subpotent Drug",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "N/A",
      "code_info": "a) Lot # D2402430, D2402431, Exp Date: 10/31/2026. b) Lot #: D2402432, Exp. Date 10/31/2026; D2500180, Exp. Date 12/31/2026.",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0785-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0786-2026",
      "event_id": "99584",
      "recalling_firm": "ACCORD HEALTHCARE, INC.",
      "product_description": "Levothyroxine Sodium Tablets, USP, 300 mcg (0.3 mg), 90-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-458-15.",
      "reason_for_recall": "Subpotent Drug",
      "distribution_pattern": "Nationwide within the United States",
      "product_quantity": "N/A",
      "code_info": "Lot #: D2402337, Exp. Date 10/31/2026.",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0786-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "D-0803-2026",
      "event_id": "99570",
      "recalling_firm": "Mallinckrodt Hospital Products Inc.",
      "product_description": "Acthar Gel (repository corticotropin injection), 5 mL multiple-dose vial, Rx Only, Mfd. for: Mallinckrodt ARD LLC, Bridgewater, NJ 08807, NDC 63004-8710-1 & NDC 63004-8710-2",
      "reason_for_recall": "Presence of particulate matter: glass and stopper piece",
      "distribution_pattern": "USA Nationwide",
      "product_quantity": "12367 vials",
      "code_info": "Lot#: NDC 63004-8710-1 - 1564-107, exp 1/31/2027 NDC 63004-8710-2 - 1564-107H, exp 1/31/2027",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0803-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "Z-3033-2026",
      "event_id": "99596",
      "recalling_firm": "IMRIS Imaging Inc",
      "product_description": "ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz Covered Table Assy V2 Part Number 114148-000",
      "reason_for_recall": "The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement occurs during a procedure.",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden.",
      "product_quantity": "6 units",
      "code_info": "113821-600 - Serial Numbers: 10003754, 10006997; 114148-000 - UDI-DI: 00857534006349, Serial Numbers: 10005189, 10005190, 10004463, 10004997",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3033-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-06",
      "recall_number": "Z-3034-2026",
      "event_id": "99596",
      "recalling_firm": "IMRIS Imaging Inc",
      "product_description": "ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600",
      "reason_for_recall": "The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement occurs during a procedure.",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden.",
      "product_quantity": "13 units",
      "code_info": "114093-000 - UDI-DI: 00857534006356, Serial Numbers: 10005695, 10002998, 10002997, 10005456, 10005612, 10004372, 10005613, 10002841, 10011119; 114093-600 - UDI-DI: 00857534006462, Serial Numbers: 10002996, 10004515, 10007411, 10007376",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3034-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class I",
      "status": "Terminated",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-04",
      "recall_number": "H-1258-2026",
      "event_id": "99571",
      "recalling_firm": "H & U Inc. dba Sun Noodle",
      "product_description": "Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net wt. 15.4oz. Product is ramen noodle kit which contains noodles and Soba soup packet. Item #05410 retail package, UPC 085315054108 Item #05410.1 cardboard box (12 packages per case), UPC 085315054105 Product is Perishable Frozen or Refrigerated and made by Sun Noodle Hawaii 1933 Colburn Street, Honolulu, HI",
      "reason_for_recall": "Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish species are not declared on finished product label.",
      "distribution_pattern": "Distribute in HI.",
      "product_quantity": "140 packages",
      "code_info": "Production Lot: 1226183 Products will be dated for expiration according to their date of defrost by retailer or distributor in the following format: MM/DD",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1258-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-04",
      "recall_number": "Z-3014-2026",
      "event_id": "99222",
      "recalling_firm": "Canon Medical System, USA, INC.",
      "product_description": "Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.",
      "reason_for_recall": "Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.",
      "distribution_pattern": "U.S. Nationwide distribution in the states of CA, GA, MN, NC, NV, PA, OH, and TX.",
      "product_quantity": "10 systems",
      "code_info": "Model Number: INFX-8000C/B3 UDI code: Pending SID Number:30101165 Serial Number: B3E2422005 Model Number: INFX-8000F/SG UDI code: Pending SID Number: 30093711 Serial Number: SGC2412001 Model Number: INFX-8000V/SZ UDI code: Pending SID Number: 30029686 Serial Number: SZA2422001 SID Number: 79000002 Serial Number:SZA2442004 Model Number: INFX-8000V/SX UDI code: Pending SID Number: 30049491 Serial Number: SXA2432001 SID Number: 30100053 Serial Number: SXA2432002 Model Number: INFX-8000V/B9 UDI code: Pending SID Number: 30059175 Serial Number: B9F2412001 Model Number: INFX-8000V/ST UDI code: Pending SID Number: 30059180 Serial Number: STA2412001 Model Number: INFX-8000V/SZ UDI code: Pending SID Number: 30095017 Serial Number: SZA2432003 SID Number: 30097052 Serial Number: SZA2422002",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3014-2026%22"
    },
    {
      "category": "Drugs",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-08-03",
      "recall_number": "D-0789-2026",
      "event_id": "99544",
      "recalling_firm": "Lupin Pharmaceuticals Inc.",
      "product_description": "Clobetasol Propionate Cream USP, 0.05%, 60 g tube, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, United States, Manufactured by: Lupin Limited, Pithampur (MP) 454 775, INDIA, NDC 68180-956-04.",
      "reason_for_recall": "Failed content uniformity specifications.",
      "distribution_pattern": "USA Nationwide",
      "product_quantity": "5082 tubes",
      "code_info": "Lot#: KB00427, Exp date 4/30/2028; KA00308, Exp date 10/31/2026",
      "source_record_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0789-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-22",
      "recall_number": "H-1274-2026",
      "event_id": "99493",
      "recalling_firm": "Lidl US TRADING",
      "product_description": "ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling. Product is packed onto a plastic carton tray with outer paper sleeve, 330 g (weight), UPC: 4056489125839.",
      "reason_for_recall": "The firm discovered that certain units shipped to the U.S. retail stores only has \"foreign languages\" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut).",
      "distribution_pattern": "Product was shipped to the following states: DC, DE, GA, MD, NJ, NY, NC, PA, SC, & VA.",
      "product_quantity": "500 units",
      "code_info": "BEST BEFORE: 10/11/2026 LOT NO: 260315",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1274-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-22",
      "recall_number": "H-1275-2026",
      "event_id": "99493",
      "recalling_firm": "Lidl US TRADING",
      "product_description": "ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with coconut sprinkles. Product is packed onto a plastic carton tray with outer paper sleeve, 330 g (weight), UPC: 4056489125846.",
      "reason_for_recall": "The firm discovered that certain units shipped to the U.S. retail stores only has \"foreign languages\" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut).",
      "distribution_pattern": "Product was shipped to the following states: DC, DE, GA, MD, NJ, NY, NC, PA, SC, & VA.",
      "product_quantity": "200 units",
      "code_info": "BEST BEFORE: 10/11/2026 LOT NO: 260315",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1275-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-22",
      "recall_number": "Z-3004-2026",
      "event_id": "99520",
      "recalling_firm": "Merge Healthcare, Inc.",
      "product_description": "Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation",
      "reason_for_recall": "Software issue may cause measurements to be displayed inaccurately.",
      "distribution_pattern": "US Nationwide distribution in the states of California, Florida, Kentucky, Nebraska, Washington.",
      "product_quantity": "20 units",
      "code_info": "Software version V9.5 - UDI (01)00842000101239(10)9.5.0(11)260409",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3004-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class I",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-13",
      "recall_number": "H-1259-2026",
      "event_id": "99424",
      "recalling_firm": "KHONG GUAN (HQ)",
      "product_description": "Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053",
      "reason_for_recall": "Undeclared peanuts.",
      "distribution_pattern": "Domestic: AZ, CA, CO, HI, NJ, OR, TX, WA. Foreign: Not applicable.",
      "product_quantity": "87 cases (36 units/case)",
      "code_info": "USE BY: 10/19/2027; 9/22/2027",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1259-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-13",
      "recall_number": "Z-2992-2026",
      "event_id": "99403",
      "recalling_firm": "Medline Industries, LP",
      "product_description": "Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007 (Teleflex Product Number/SKU 780-07); 2) HUDSON RCI, DBM-CIRCUIT,VENT,NEONATAL,21 V, Medline Product Number/SKU HUD78009 (Teleflex Product Number/SKU 780-09); 3) HUDSON RCI, DBD-CIRCUIT,VENT,INSIRATORY,HEATED,NEO,4, Medline Product Number/SKU 780-13 (Teleflex Product Number/SKU 780-13); 4) HUDSON RCI, DBD-CIRCUIT,VENT,INSIRATORY,HEATED,NEO,4, Medline Product Number/SKU 780-14 (Teleflex Product Number/SKU 780-14); 5) HUDSON RCI, DBD-CIRCUIT, HTD, DUAL LIMB, NEONATE, Medline Product Number/SKU 780-15 (Teleflex Product Number/SKU 780-15); 6) HUDSON RCI, CIRCUIT,NEO,DUAL,WIRE,60 IN, Medline Product Number/SKU HUD7801780-18) (Teleflex Product Number/SKU 780-18).",
      "reason_for_recall": "Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage. Device failure may predispose infant to bronchospasm, inspissated secretions, and airway obstruction, as well as inadvertent positive end-expiratory pressure (PEEP), circuit obstruction, or accidental lavage of pooled fluid into the airway, elevated oxygen consumption, and worsening respiratory distress.",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Panama.",
      "product_quantity": "145525 units",
      "code_info": "1) Medline Product Number/SKU HUD78007, UDI/DI 10197344042463 (each) 20197344042460 (case), All lot numbers; 2) Medline Product Number/SKU HUD78009, UDI/DI Discontinued (each) Discontinued (case), All lot numbers; 3) Medline Product Number/SKU 780-13, UDI/DI Discontinued (each) Discontinued (case), All lot numbers; 4) Medline Product Number/SKU 780-14, UDI/DI Discontinued (each) Discontinued (case), All lot numbers; 5) Medline Product Number/SKU 780-15, UDI/DI Discontinued (each) Discontinued (case), All lot numbers; 6) Medline Product Number/SKU HUD78018, UDI/DI 10197344010660 (each) 20197344010667 (case), All lot numbers.",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2992-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-10",
      "recall_number": "Z-3022-2026",
      "event_id": "99507",
      "recalling_firm": "Medline Industries, LP",
      "product_description": "Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U; 2) OPERATIVE LAP P&S SURGICAL, Medline Kit SKU DYNJ89608; 3) LAPAROSCOPY, Medline Kit SKU DYNJ903479L; 4) LAPAROSCOPY, Medline Kit SKU DYNJ903479M.",
      "reason_for_recall": "Kits contain a potentially contaminated component which were recalled by the manufacturer",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.",
      "product_quantity": "94 kits",
      "code_info": "Medline Kit SKU CDS982040U, UDI/DI 10198459385421 (each) 40198459385422 (case), Lot Number 26AMC355; Medline Kit SKU DYNJ89608, UDI/DI 10198459279324 (each) 40198459279325 (case), Lot Number 25JBR465; Medline Kit SKU DYNJ903479L, UDI/DI 10198459255250 (each) 40198459255251 (case), Lot Number 25LMB480; Medline Kit SKU DYNJ903479M, UDI/DI 10198459790591 (each) 40198459790592 (case), Lot Number 26FMB173.",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3022-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-10",
      "recall_number": "Z-3026-2026",
      "event_id": "99507",
      "recalling_firm": "Medline Industries, LP",
      "product_description": "Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L; 2) C-SECTION, Medline Kit SKU DYNJ911755; 3) AHR C-SECTION KIT, Medline Kit SKU DYNJ912014.",
      "reason_for_recall": "Kits contain a potentially contaminated component which were recalled by the manufacturer",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.",
      "product_quantity": "106 kits",
      "code_info": "Medline Kit SKU DYNJ904612L, UDI/DI 10198459495625 (each) 40198459495626 (case), Lot Number 26FMC710; Medline Kit SKU DYNJ904612L, UDI/DI 10198459495625 (each) 40198459495626 (case), Lot Number 26DMG417; Medline Kit SKU DYNJ911755, UDI/DI 10198459523946 (each) 40198459523947 (case), Lot Number 25KMI628; Medline Kit SKU DYNJ912014, UDI/DI 10198459599569 (each) 40198459599560 (case), Lot Number 26ABJ549; Medline Kit SKU DYNJ912014, UDI/DI 10198459599569 (each) 40198459599560 (case), Lot Number 26ABI899; Medline Kit SKU DYNJ912014, UDI/DI 10198459599569 (each) 40198459599560 (case), Lot Number 25LBT433.",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3026-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-10",
      "recall_number": "Z-3028-2026",
      "event_id": "99507",
      "recalling_firm": "Medline Industries, LP",
      "product_description": "Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU DYNJ54362F; 2) EAST MAJOR LITHOTOMY, Medline Kit SKU DYNJ900957C; 3) GYN LAPAROTOMY, Medline Kit SKU DYNJ906804B; 4) UNIVERSAL GYN, Medline Kit SKU DYNJ910195A.",
      "reason_for_recall": "Kits contain a potentially contaminated component which were recalled by the manufacturer",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.",
      "product_quantity": "419 kits",
      "code_info": "Medline Kit SKU DYNJ54362F, UDI/DI 10198459794292 (each) 40198459794293 (case), Lot Number 26EMF986; Medline Kit SKU DYNJ900957C, UDI/DI 10195327599461 (each) 40195327599462 (case), Lot Number 25IBP434; Medline Kit SKU DYNJ906804B, UDI/DI 10195327433376 (each) 40195327433377 (case), Lot Number 26BBA665; Medline Kit SKU DYNJ906804B, UDI/DI 10195327433376 (each) 40195327433377 (case), Lot Number 25KBR602; Medline Kit SKU DYNJ906804B, UDI/DI 10195327433376 (each) 40195327433377 (case), Lot Number 25JBH531; Medline Kit SKU DYNJ910195A, UDI/DI 10198459556838 (each) 40198459556839 (case), Lot Number 25KBL876; Medline Kit SKU DYNJ910195A, UDI/DI 10198459556838 (each) 40198459556839 (case), Lot Number 25JBS218.",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3028-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-10",
      "recall_number": "Z-3029-2026",
      "event_id": "99507",
      "recalling_firm": "Medline Industries, LP",
      "product_description": "Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT CRANIOTOMY RFD, Medline Kit SKU DYNJ906496K.",
      "reason_for_recall": "Kits contain a potentially contaminated component which were recalled by the manufacturer",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.",
      "product_quantity": "241 kits",
      "code_info": "Medline Kit SKU CDS982035Y, UDI/DI 10198459385636 (each) 40198459385637 (case), Lot Number 25LMF531; Medline Kit SKU CDS982035Y, UDI/DI 10198459385636 (each) 40198459385637 (case), Lot Number 25JML577; Medline Kit SKU DYNJT6104, UDI/DI 10198459539374 (each) 40198459539375 (case), Lot Number 25JBM473; Medline Kit SKU DYNJ903471I, UDI/DI 10198459255069 (each) 40198459255060 (case), Lot Number 26DDB085; Medline Kit SKU DYNJ903471I, UDI/DI 10198459255069 (each) 40198459255060 (case), Lot Number 26DDA481; Medline Kit SKU DYNJ903471I, UDI/DI 10198459255069 (each) 40198459255060 (case), Lot Number 26CDA102; Medline Kit SKU DYNJ906496K, UDI/DI 10198459419614 (each) 40198459419615 (case), Lot Number 25KLA074.",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3029-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-07-08",
      "recall_number": "Z-2994-2026",
      "event_id": "99489",
      "recalling_firm": "Medline Industries, LP",
      "product_description": "Medline medical convenience kits, labeled as: 1) SINUS PACK-LF, Medline Kit SKU DYNJ0966146F; 2) ENT PACK, Medline Kit SKU DYNJ40154D; 3) ENT PACK, Medline Kit SKU DYNJ40154F; 4) ENT SCOPE PACK, Medline Kit SKU DYNJ44480D; 5) ENT NASAL ORAL PACK MOSES, Medline Kit SKU DYNJ58928A; 6) HEAD & NECK PACK, Medline Kit SKU DYNJ83296; 7) TRANSPHENOIDAL PACK, Medline Kit SKU DYNJ89006; 8) SINUS, Medline Kit SKU DYNJ900537D; 9) SINUS, Medline Kit SKU DYNJ900537F; 10) ENT HEAD & NECK, Medline Kit SKU DYNJ903679F; 11) ENT HEAD & NECK, Medline Kit SKU DYNJ903679G; 12) ENT HEAD & NECK, Medline Kit SKU DYNJ903679I; 13) ENT HEAD & NECK, Medline Kit SKU DYNJ903679J; 14) ENT HEAD & NECK, Medline Kit SKU DYNJ903679K.",
      "reason_for_recall": "Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, IA, ID, IL, IN, MA, MD, MI, MN, MO, MT, NY, OH, TX, WI, WY.",
      "product_quantity": "2262 kits",
      "code_info": "Medline Kit SKU DYNJ0966146F, UDI/DI 10193489916379 (each) 40193489916370 (case), Lot Number 23HBC070; Medline Kit SKU DYNJ40154D, UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 24CBA416; Medline Kit SKU DYNJ40154D, UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 23CBS214; Medline Kit SKU DYNJ40154D, UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 23FBC803; Medline Kit SKU DYNJ40154D, UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 23GBU042; Medline Kit SKU DYNJ40154D, UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 23IBO417; Medline Kit SKU DYNJ40154F, UDI/DI 10195327679293 (each) 40195327679294 (case), Lot Number 24EBH594; Medline Kit SKU DYNJ40154F, UDI/DI 10195327679293 (each) 40195327679294 (case), Lot Number 24FBQ494; Medline Kit SKU DYNJ40154F, UDI/DI 10195327679293 (each) 40195327679294 (case), Lot Number 24JBK316; Medline Kit SKU DYNJ44480D, UDI/DI 10198459241727 (each) 40198459241728 (case), Lot Number 25CDA135; Medline Kit SKU DYNJ58928A, UDI/DI 10193489763973 (each) 40193489763974 (case), Lot Number 23HBK833; Medline Kit SKU DYNJ83296, UDI/DI 10195327258917 (each) 40195327258918 (case), Lot Number 24FBQ476; Medline Kit SKU DYNJ83296, UDI/DI 10195327258917 (each) 40195327258918 (case), Lot Number 23EBI941; Medline Kit SKU DYNJ83296, UDI/DI 10195327258917 (each) 40195327258918 (case), Lot Number 23HBX888; Medline Kit SKU DYNJ83296, UDI/DI 10195327258917 (each) 40195327258918 (case), Lot Number 22KBR883; Medline Kit SKU DYNJ89006, UDI/DI 10198459241970 (each) 40198459241971 (case), Lot Number 25JMC017; Medline Kit SKU DYNJ89006, UDI/DI 10198459241970 (each) 40198459241971 (case), Lot Number 25KMB183; Medline Kit SKU DYNJ89006, UDI/DI 10198459241970 (each) 40198459241971 (case), Lot Number 25AMG343; Medline Kit SKU DYNJ89006, UDI/DI 10198459241970 (each) 40198459241971 (case), Lot Number 25DMJ252; Medline Kit SKU DYNJ900537D, UDI/DI 10888277775206 (each) 40888277775207 (case), Lot Number 23ABM594; Medline Kit SKU DYNJ900537D, UDI/DI 10888277775206 (each) 40888277775207 (case), Lot Number 23DBQ757; Medline Kit SKU DYNJ900537D, UDI/DI 10888277775206 (each) 40888277775207 (case), Lot Number 23EBL559; Medline Kit SKU DYNJ900537D, UDI/DI 10888277775206 (each) 40888277775207 (case), Lot Number 22FBC585; Medline Kit SKU DYNJ900537D, UDI/DI 10888277775206 (each) 40888277775207 (case), Lot Number 22GBO880; Medline Kit SKU DYNJ900537D, UDI/DI 10888277775206 (each) 40888277775207 (case), Lot Number 22HBN179; Medline Kit SKU DYNJ900537D, UDI/DI 10888277775206 (each) 40888277775207 (case), Lot Number 22HBU967; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 25CME312; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 25FME826; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 24IMA157; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 24IMF249; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 23EBI617; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 23GBJ097; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 23HBS862; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 23JBU735; Medline Kit SKU DYNJ900537F, UDI/DI 10195327397371 (each) 40195327397372 (case), Lot Number 23KBI060; Medline Kit SKU DYNJ903679F, UDI/DI 10195327182908 (each) 40195327182909 (case), Lot Number 23ABS340; Medline Kit SKU DYNJ903679F, UDI/DI 10195327182908 (each) 40195327182909 (case), Lot Number 23ABS768; Medline Kit SKU DYNJ903679F, UDI/DI 10195327182908 (each) 40195327182909 (case), Lot Number 23BBB045; Medline Kit SKU DYNJ903679F, UDI/DI 10195327182908 (each) 40195327182909 (case), Lot Number 23HBP969; Medline Kit SKU DYNJ903679F, UDI/DI 10195327182908 (each) 40195327182909 (case), Lot Number 22HBR343; Medline Kit SKU DYNJ903679F, UDI/DI 10195327182908 (each) 40195327182909 (case), Lot Number 22HBT245; Medline Kit SKU DYNJ903679F, UDI/DI 10195327182908 (each) 40195327182909 (case), Lot Number 22LBL269; Medline Kit SKU DYNJ903679G, UDI/DI 10195327488093 (each) 40195327488094 (case), Lot Number 24DBD707; Medline Kit SKU DYNJ903679G, UDI/DI 10195327488093 (each) 40195327488094 (case), Lot Number 24DBD912; Medline Kit SKU DYNJ903679G, UDI/DI 10195327488093 (each) 40195327488094 (case), Lot Number 24HBR037; Medline Kit SKU DYNJ903679G, UDI/DI 10195327488093 (each) 40195327488094 (case), Lot Number 24IBF556; Medline Kit SKU DYNJ903679G, UDI/DI 10195327488093 (each) 40195327488094 (case), Lot Number 24JBM973; Medline Kit SKU DYNJ903679G, UDI/DI 10195327488093 (each) 40195327488094 (case), Lot Number 23LBG405; Medline Kit SKU DYNJ903679I, UDI/DI 10198459225758 (each) 40198459225759 (case), Lot Number 25BBD293; Medline Kit SKU DYNJ903679I, UDI/DI 10198459225758 (each) 40198459225759 (case), Lot Number 25BBF473; Medline Kit SKU DYNJ903679I, UDI/DI 10198459225758 (each) 40198459225759 (case), Lot Number 25BBF871; Medline Kit SKU DYNJ903679J, UDI/DI 10198459313035 (each) 40198459313036 (case), Lot Number 25DBU804; Medline Kit SKU DYNJ903679J, UDI/DI 10198459313035 (each) 40198459313036 (case), Lot Number 25EBN687; Medline Kit SKU DYNJ903679J, UDI/DI 10198459313035 (each) 40198459313036 (case), Lot Number 25FBR466; Medline Kit SKU DYNJ903679K, UDI/DI 10198459399916 (each) 40198459399917 (case), Lot Number 25HBF447; Medline Kit SKU DYNJ903679K, UDI/DI 10198459399916 (each) 40198459399917 (case), Lot Number 25KBT345.",
      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2994-2026%22"
    },
    {
      "category": "Devices",
      "classification": "Class II",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-06-30",
      "recall_number": "Z-3017-2026",
      "event_id": "99438",
      "recalling_firm": "Fresenius Medical Care Renal Therapies Group, LLC",
      "product_description": "Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine, Model Numbers: 191126, 191130.",
      "reason_for_recall": "Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis machines.",
      "distribution_pattern": "US Nationwide distribution.",
      "product_quantity": "1140 systems",
      "code_info": "191126, UDI/DI 00840861102099, Serial Numbers: 5T0S291116, 5T0S291119, 5T0S291125, 5T0S291135, 5T0S291137, 5T0S291138, 5T0S291139, 5T0S291140, 5T0S291141, 5T0S291143, 5T0S291144, 5T0S291145, 5T0S291146, 5T0S291148, 5T0S291149, 5T0S291150, 5T0S291151, 5T0S291152, 5T0S291154, 5T0S291155, 5T0S291156, 5T0S291157, 5T0S291158, 5T0S291159, 5T0S291160, 5T0S291161, 5T0S291162, 5T0S291163, 5T0S291164, 5T0S291165, 5T0S291166, 5T0S291168, 5T0S291169, 5T0S291170, 5T0S291173, 5T0S291177, 5T0S291178, 5T0S291179, 5T0S291180, 5T0S291181, 5T0S291182, 5T0S291183, 5T0S291184, 5T0S291185, 5T0S291186, 5T0S291187, 5T0S291188, 5T0S291189, 5T0S291190, 5T0S291191, 5T0S291192, 5T0S291193, 5T0S291194, 5T0S291195, 5T0S291196, 5T0S291197, 5T0S291198, 5T0S291199, 5T0S291200, 5T0S291201, 5T0S291202, 5T0S291203, 5T0S291204, 5T0S291205, 5T0S291206, 5T0S291207, 5T0S291208, 5T0S291209, 5T0S291210, 5T0S291211, 5T0S291212, 5T0S291213, 5T0S291214, 5T0S291215, 5T0S291216, 5T0S291217, 5T0S291218, 5T0S291219, 5T0S291220, 5T0S291221, 5T0S291222, 5T0S291223, 5T0S291224, 5T0S291225, 5T0S291226, 5T0S291228, 5T0S291229, 5T0S291230, 5T0S291231, 5T0S291232, 5T0S291234, 5T0S291235, 5T0S291242, 5T0S291243, 5T0S291244, 5T0S291245, 5T0S291247, 5T0S291248, 5T0S291249, 5T0S291250, 5T0S291251, 5T0S291252, 5T0S291253, 5T0S291314, 5T0S291315, 5T0S291316, 5T0S291317, 5T0S291318, 5T0S291319, 5T0S291320, 5T0S291321, 5T0S291322, 5T0S291323, 5T0S291324, 5T0S291325, 5T0S291326, 5T0S291327, 5T0S291328, 5T0S291329, 5T0S291330, 5T0S291332, 5T0S291333, 5T0S291334, 5T0S291335, 5T0S291337, 5T0S291338, 5T0S291339, 5T0S291340, 5T0S291341, 5T0S291342, 5T0S291343, 5T0S291346, 5T0S291403, 5T0S291407, 5T0S291408, 5T0S291409, 5T0S291410, 5T0S291411, 5T0S291412, 5T0S291413, 5T0S291414, 5T0S291415, 5T0S291416, 5T0S291417, 5T0S291418, 5T0S291421, 5T0S291423, 5T0S291424, 5T0S291425, 5T0S291426, 5T0S291427, 5T0S291428, 5T0S291433, 5T0S291435, 5T0S291436, 5T0S291438, 5T0S291440, 5T0S291441, 5T0S291442, 5T0S291444, 5T0S291446, 5T0S291447, 5T0S291450, 5T0S291452, 5T0S291458, 5T0S291460, 5T0S291461, 5T0S291463, 5T0S291464, 5T0S291466, 5T0S291467, 5T0S291472, 5T0S291474, 5T0S291476, 5T0S291479, 5T0S291480, 5T0S291526, 5T0S291556, 5T0S291584, 6T0S292446, 6T0S292448, 6T0S292460, 6T0S292461, 6T0S292463, 6T0S292464, 6T0S292465, 6T0S292466, 6T0S292467, 6T0S292468, 6T0S292469, 6T0S292470, 6T0S292471, 6T0S292472, 6T0S292473, 6T0S292474, 6T0S292475, 6T0S292476, 6T0S292477, 6T0S292478, 6T0S292479, 6T0S292480, 6T0S292481, 6T0S292482, 6T0S292483, 6T0S292484, 6T0S292485, 6T0S292486, 6T0S292487, 6T0S292488, 6T0S292489, 6T0S292490, 6T0S292491, 6T0S292492, 6T0S292493, 6T0S292494, 6T0S292495, 6T0S292496, 6T0S292498, 6T0S292499, 6T0S292500, 6T0S292501, 6T0S292502, 6T0S292503, 6T0S292504, 6T0S292505, 6T0S292506, 6T0S292507, 6T0S292508, 6T0S292509, 6T0S292510, 6T0S292511, 6T0S292512, 6T0S292513, 6T0S292514, 6T0S292515, 6T0S292516, 6T0S292517, 6T0S292518, 6T0S292519, 6T0S292520, 6T0S292521, 6T0S292522, 6T0S292523, 6T0S292524, 6T0S292525, 6T0S292526. 191130, UDI/DI 00840861102112, Serial Numbers: 6T0S291719, 6T0S291816, 6T0S291842, 6T0S291844, 6T0S291850, 6T0S291856, 6T0S291857, 6T0S291859, 6T0S291861, 6T0S291874, 6T0S291884, 6T0S291893, 6T0S291899, 6T0S291901, 6T0S291902, 6T0S291903, 6T0S291904, 6T0S291905, 6T0S291906, 6T0S291907, 6T0S291908, 6T0S291909, 6T0S291910, 6T0S291911, 6T0S291912, 6T0S291913, 6T0S291914, 6T0S291915, 6T0S291916, 6T0S291917, 6T0S291918, 6T0S291919, 6T0S291920, 6T0S291921, 6T0S291922, 6T0S291923, 6T0S291924, 6T0S291925, 6T0S291926, 6T0S291927, 6T0S291928, 6T0S291929, 6T0S291930, 6T0S291931, 6T0S291932, 6T0S291933, 6T0S291934, 6T0S291935, 6T0S291936, 6T0S291937, 6T0S291938, 6T0S291939, 6T0S291940, 6T0S291941, 6T0S291942, 6T0S291943, 6T0S291944, 6T0S291945, 6T0S291946, 6T0S291947, 6T0S291948, 6T0S291949, 6T0S291950, 6T0S291951, 6T0S291952, 6T0S291953, 6T0S291954, 6T0S291955, 6T0S291956, 6T0S291957, 6T0S291958, 6T0S291959, 6T0S291960, 6T0S291961, 6T0S291962, 6T0S291963, 6T0S291964, 6T0S291965, 6T0S291966, 6T0S291967, 6T0S291968, 6T0S291969, 6T0S291970, 6T0S291971, 6T0S291972, 6T0S291973, 6T0S291974, 6T0S291975, 6T0S291976, 6T0S291977, 6T0S291978, 6T0S291979, 6T0S291980, 6T0S291981, 6T0S291982, 6T0S291983, 6T0S291984, 6T0S291985, 6T0S291986, 6T0S291987, 6T0S291988, 6T0S291989, 6T0S291990, 6T0S291991, 6T0S291992, 6T0S291993, 6T0S291994, 6T0S291995, 6T0S291996, 6T0S291997, 6T0S291998, 6T0S291999, 6T0S292000, 6T0S292001, 6T0S292002, 6T0S292003, 6T0S292004, 6T0S292005, 6T0S292006, 6T0S292007, 6T0S292008, 6T0S292009, 6T0S292010, 6T0S292042, 6T0S292043, 6T0S292044, 6T0S292045, 6T0S292046, 6T0S292047, 6T0S292048, 6T0S292049, 6T0S292050, 6T0S292051, 6T0S292052, 6T0S292053, 6T0S292054, 6T0S292055, 6T0S292056, 6T0S292057, 6T0S292058, 6T0S292059, 6T0S292060, 6T0S292061, 6T0S292062, 6T0S292063, 6T0S292064, 6T0S292065, 6T0S292066, 6T0S292067, 6T0S292069, 6T0S292074, 6T0S292075, 6T0S292076, 6T0S292077, 6T0S292079, 6T0S292080, 6T0S292081, 6T0S292082, 6T0S292083, 6T0S292084, 6T0S292085, 6T0S292087, 6T0S292088, 6T0S292089, 6T0S292090, 6T0S292091, 6T0S292092, 6T0S292093, 6T0S292094, 6T0S292095, 6T0S292096, 6T0S292097, 6T0S292098, 6T0S292099, 6T0S292100, 6T0S292101, 6T0S292102, 6T0S292103, 6T0S292104, 6T0S292105, 6T0S292106, 6T0S292107, 6T0S292108, 6T0S292109, 6T0S292110, 6T0S292111, 6T0S292112, 6T0S292113, 6T0S292114, 6T0S292115, 6T0S292116, 6T0S292117, 6T0S292118, 6T0S292119, 6T0S292120, 6T0S292121, 6T0S292122, 6T0S292123, 6T0S292124, 6T0S292125, 6T0S292126, 6T0S292127, 6T0S292128, 6T0S292129, 6T0S292130, 6T0S292131, 6T0S292132, 6T0S292133, 6T0S292134, 6T0S292135, 6T0S292136, 6T0S292137, 6T0S292138, 6T0S292139, 6T0S292140, 6T0S292141, 6T0S292142, 6T0S292143, 6T0S292144, 6T0S292145, 6T0S292146, 6T0S292147, 6T0S292148, 6T0S292149, 6T0S292150, 6T0S292151, 6T0S292152, 6T0S292153, 6T0S292154, 6T0S292155, 6T0S292156, 6T0S292157, 6T0S292158, 6T0S292159, 6T0S292160, 6T0S292161, 6T0S292162, 6T0S292163, 6T0S292164, 6T0S292165, 6T0S292166, 6T0S292167, 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      "source_record_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3017-2026%22"
    },
    {
      "category": "Food",
      "classification": "Class I",
      "status": "Ongoing",
      "report_date": "2026-09-02",
      "recall_initiation_date": "2026-04-03",
      "recall_number": "H-1263-2026",
      "event_id": "98691",
      "recalling_firm": "ZMB Enterprises",
      "product_description": "Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement",
      "reason_for_recall": "The product contains 1,4-DMAA, Phenylethylamine and Phenibut.",
      "distribution_pattern": "The firm markets their products online via their website addallxr.com",
      "product_quantity": "unknown",
      "code_info": "Sold between July - December 2025",
      "source_record_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1263-2026%22"
    }
  ]
}