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  <title>Recall Radar latest recalls</title>
  <subtitle>Recent FDA food, drug, supplement, and medical device recalls from public openFDA enforcement data.</subtitle>
  <link href="https://notyetneeded.com/latest-recalls" rel="alternate" type="text/html"/>
  <link href="https://notyetneeded.com/atom.xml" rel="self" type="application/atom+xml"/>
  <updated>2026-09-07T22:36:03.503Z</updated>
  <author>
    <name>Not Yet Needed</name>
  </author>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0831-2026</id>
    <title>Drugs: Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05) bott...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0831-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Hikma Pharmaceuticals USA INC. | Reason: Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU). | Distribution: Nationwide within the United States | Recall began: 2026-08-24 | FDA IDs: D-0831-2026 / event 99711</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1264-2026</id>
    <title>Food: Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fr...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1264-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Dreyer&#39;s Grand Ice Cream Inc. | Reason: Foreign object: products may contain glass pieces | Distribution: 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. | Recall began: 2026-08-18 | FDA IDs: H-1264-2026 / event 99716</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1265-2026</id>
    <title>Food: Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual frui...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1265-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Dreyer&#39;s Grand Ice Cream Inc. | Reason: Foreign object: products may contain glass pieces | Distribution: 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. | Recall began: 2026-08-18 | FDA IDs: H-1265-2026 / event 99716</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1266-2026</id>
    <title>Food: Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit b...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1266-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Dreyer&#39;s Grand Ice Cream Inc. | Reason: Foreign object: products may contain glass pieces | Distribution: 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. | Recall began: 2026-08-18 | FDA IDs: H-1266-2026 / event 99716</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1268-2026</id>
    <title>Food: Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in paper outer cartons; individual...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1268-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Dreyer&#39;s Grand Ice Cream Inc. | Reason: Foreign object: products may contain glass pieces | Distribution: 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. | Recall began: 2026-08-18 | FDA IDs: H-1268-2026 / event 99716</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3035-2026</id>
    <title>Devices: POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer &amp; Divider, Double Action. GEI / Electrosurgical, cutting &amp;...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3035-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Olympus Corporation of the Americas | Reason: Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. | Distribution: Worldwide - US Nationwide distribution in the states of Kansas and Florida. The countries of Australia, European Union, Japan. | Recall began: 2026-08-18 | FDA IDs: Z-3035-2026 / event 99607</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1271-2026</id>
    <title>Food: Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons &amp; White Cheddar Cheese, Ready to Heat, Net Wt. 14...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1271-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: CUISINE, KETTLE | Reason: Product had a presumptive positive test result for Listeria monocytogenes | Distribution: The recalled product was distributed to the following States: IL, NV, NM, CA, OK, TX, PA, OH, NC, NY, GA, and AR. | Recall began: 2026-08-11 | FDA IDs: H-1271-2026 / event 99690</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1278-2026</id>
    <title>Food: Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formula...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1278-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Byron White Formulas, Inc. | Reason: Label does not declare walnuts in English | Distribution: 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, S... | Recall began: 2026-08-11 | FDA IDs: H-1278-2026 / event 99629</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0790-2026</id>
    <title>Drugs: Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol &amp; Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0790-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Church &amp; Dwight Co., Inc. | Reason: CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing | Distribution: US Nationwide. | Recall began: 2026-08-10 | FDA IDs: D-0790-2026 / event 99604</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/N/A</id>
    <title>Food: Clear glass bottle with black screw lid with multi label which reads in part as &quot;***AFRICANDO FOODS, LLC ALFREDO HOT SAU...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22N%2FA%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Not Yet Classified | Ongoing | Firm: Africando Foods LLC | Reason: Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list | Distribution: 8 wholesale and retail locations in IA, KY and IL | Recall began: 2026-08-10 | FDA IDs: N/A / event 99642</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0775-2026</id>
    <title>Drugs: Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare,...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0775-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: ACCORD HEALTHCARE, INC. | Reason: Subpotent Drug | Distribution: Nationwide within the United States | Recall began: 2026-08-06 | FDA IDs: D-0775-2026 / event 99584</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0776-2026</id>
    <title>Drugs: Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, I...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0776-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: ACCORD HEALTHCARE, INC. | Reason: Subpotent Drug | Distribution: Nationwide within the United States | Recall began: 2026-08-06 | FDA IDs: D-0776-2026 / event 99584</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0777-2026</id>
    <title>Drugs: Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare,...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0777-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: ACCORD HEALTHCARE, INC. | Reason: Subpotent Drug | Distribution: Nationwide within the United States | Recall began: 2026-08-06 | FDA IDs: D-0777-2026 / event 99584</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0781-2026</id>
    <title>Drugs: Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare,...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0781-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: ACCORD HEALTHCARE, INC. | Reason: Subpotent Drug | Distribution: Nationwide within the United States | Recall began: 2026-08-06 | FDA IDs: D-0781-2026 / event 99584</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0782-2026</id>
    <title>Drugs: Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg), packaged in a) 90-count bottles (NDC 16729-454-15) b) 1000-count...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0782-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: ACCORD HEALTHCARE, INC. | Reason: Subpotent Drug | Distribution: Nationwide within the United States | Recall began: 2026-08-06 | FDA IDs: D-0782-2026 / event 99584</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0783-2026</id>
    <title>Drugs: Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare,...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0783-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: ACCORD HEALTHCARE, INC. | Reason: Subpotent Drug | Distribution: Nationwide within the United States | Recall began: 2026-08-06 | FDA IDs: D-0783-2026 / event 99584</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0785-2026</id>
    <title>Drugs: Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg), packaged in a) 90-count bottles (NDC 16729-457-15) and b) 1000-coun...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0785-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: ACCORD HEALTHCARE, INC. | Reason: Subpotent Drug | Distribution: Nationwide within the United States | Recall began: 2026-08-06 | FDA IDs: D-0785-2026 / event 99584</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0786-2026</id>
    <title>Drugs: Levothyroxine Sodium Tablets, USP, 300 mcg (0.3 mg), 90-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0786-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: ACCORD HEALTHCARE, INC. | Reason: Subpotent Drug | Distribution: Nationwide within the United States | Recall began: 2026-08-06 | FDA IDs: D-0786-2026 / event 99584</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0803-2026</id>
    <title>Drugs: Acthar Gel (repository corticotropin injection), 5 mL multiple-dose vial, Rx Only, Mfd. for: Mallinckrodt ARD LLC, Bridg...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0803-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Mallinckrodt Hospital Products Inc. | Reason: Presence of particulate matter: glass and stopper piece | Distribution: USA Nationwide | Recall began: 2026-08-06 | FDA IDs: D-0803-2026 / event 99570</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3033-2026</id>
    <title>Devices: ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3033-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: IMRIS Imaging Inc | Reason: 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 occu... | Distribution: Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden. | Recall began: 2026-08-06 | FDA IDs: Z-3033-2026 / event 99596</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3034-2026</id>
    <title>Devices: ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3034-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: IMRIS Imaging Inc | Reason: 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 occu... | Distribution: Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden. | Recall began: 2026-08-06 | FDA IDs: Z-3034-2026 / event 99596</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1258-2026</id>
    <title>Food: Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles &amp; Soup Base. Retail package net wt. 15.4oz. Product is ramen no...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1258-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class I | Terminated | Firm: H &amp; U Inc. dba Sun Noodle | Reason: 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: Distribute in HI. | Recall began: 2026-08-04 | FDA IDs: H-1258-2026 / event 99571</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3014-2026</id>
    <title>Devices: Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluoroscopy system used in a diagn...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3014-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Canon Medical System, USA, INC. | Reason: 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: U.S. Nationwide distribution in the states of CA, GA, MN, NC, NV, PA, OH, and TX. | Recall began: 2026-08-04 | FDA IDs: Z-3014-2026 / event 99222</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/D-0789-2026</id>
    <title>Drugs: Clobetasol Propionate Cream USP, 0.05%, 60 g tube, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34...</title>
    <link href="https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0789-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Lupin Pharmaceuticals Inc. | Reason: Failed content uniformity specifications. | Distribution: USA Nationwide | Recall began: 2026-08-03 | FDA IDs: D-0789-2026 / event 99544</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1274-2026</id>
    <title>Food: ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating &amp; Apricot Filling. Product is packed onto a plas...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1274-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Lidl US TRADING | Reason: The firm discovered that certain units shipped to the U.S. retail stores only has &quot;foreign languages&quot; on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut). | Distribution: Product was shipped to the following states: DC, DE, GA, MD, NJ, NY, NC, PA, SC, &amp; VA. | Recall began: 2026-07-22 | FDA IDs: H-1274-2026 / event 99493</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1275-2026</id>
    <title>Food: ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with coconut sprinkles. Product is packe...</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1275-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Lidl US TRADING | Reason: The firm discovered that certain units shipped to the U.S. retail stores only has &quot;foreign languages&quot; on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut). | Distribution: Product was shipped to the following states: DC, DE, GA, MD, NJ, NY, NC, PA, SC, &amp; VA. | Recall began: 2026-07-22 | FDA IDs: H-1275-2026 / event 99493</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3004-2026</id>
    <title>Devices: Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3004-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Merge Healthcare, Inc. | Reason: Software issue may cause measurements to be displayed inaccurately. | Distribution: US Nationwide distribution in the states of California, Florida, Kentucky, Nebraska, Washington. | Recall began: 2026-07-22 | FDA IDs: Z-3004-2026 / event 99520</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1259-2026</id>
    <title>Food: Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1259-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class I | Ongoing | Firm: KHONG GUAN (HQ) | Reason: Undeclared peanuts. | Distribution: Domestic: AZ, CA, CO, HI, NJ, OR, TX, WA. Foreign: Not applicable. | Recall began: 2026-07-13 | FDA IDs: H-1259-2026 / event 99424</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-2992-2026</id>
    <title>Devices: Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2992-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Medline Industries, LP | Reason: 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 pr... | Distribution: Worldwide distribution - US Nationwide and the country of Panama. | Recall began: 2026-07-13 | FDA IDs: Z-2992-2026 / event 99403</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3022-2026</id>
    <title>Devices: Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U; 2) OPERATIVE LAP P&amp;S SURGICAL, Medl...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3022-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Medline Industries, LP | Reason: Kits contain a potentially contaminated component which were recalled by the manufacturer | Distribution: 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. | Recall began: 2026-07-10 | FDA IDs: Z-3022-2026 / event 99507</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3026-2026</id>
    <title>Devices: Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L; 2) C-SECTION, Medline Kit SKU DYNJ911755...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3026-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Medline Industries, LP | Reason: Kits contain a potentially contaminated component which were recalled by the manufacturer | Distribution: 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. | Recall began: 2026-07-10 | FDA IDs: Z-3026-2026 / event 99507</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3028-2026</id>
    <title>Devices: Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU DYNJ54362F; 2) EAST MAJOR LITHOTOMY, Me...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3028-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Medline Industries, LP | Reason: Kits contain a potentially contaminated component which were recalled by the manufacturer | Distribution: 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. | Recall began: 2026-07-10 | FDA IDs: Z-3028-2026 / event 99507</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3029-2026</id>
    <title>Devices: Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medlin...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3029-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Medline Industries, LP | Reason: Kits contain a potentially contaminated component which were recalled by the manufacturer | Distribution: 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. | Recall began: 2026-07-10 | FDA IDs: Z-3029-2026 / event 99507</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-2994-2026</id>
    <title>Devices: Medline medical convenience kits, labeled as: 1) SINUS PACK-LF, Medline Kit SKU DYNJ0966146F; 2) ENT PACK, Medline Kit S...</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2994-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Medline Industries, LP | Reason: 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: US Nationwide distribution in the states of AZ, CA, IA, ID, IL, IN, MA, MD, MI, MN, MO, MT, NY, OH, TX, WI, WY. | Recall began: 2026-07-08 | FDA IDs: Z-2994-2026 / event 99489</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/Z-3017-2026</id>
    <title>Devices: Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine, Model Numbers: 191126, 191130.</title>
    <link href="https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3017-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class II | Ongoing | Firm: Fresenius Medical Care Renal Therapies Group, LLC | Reason: 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: US Nationwide distribution. | Recall began: 2026-06-30 | FDA IDs: Z-3017-2026 / event 99438</summary>
  </entry>
  <entry>
    <id>https://notyetneeded.com/recalls/H-1263-2026</id>
    <title>Food: Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement</title>
    <link href="https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1263-2026%22" rel="alternate"/>
    <updated>2026-09-02T00:00:00.000Z</updated>
    <summary>Class I | Ongoing | Firm: ZMB Enterprises | Reason: The product contains 1,4-DMAA, Phenylethylamine and Phenibut. | Distribution: The firm markets their products online via their website addallxr.com | Recall began: 2026-04-03 | FDA IDs: H-1263-2026 / event 98691</summary>
  </entry>
</feed>
