BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Not Yet Needed//Recall Radar//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Recall Radar latest recalls
X-WR-CALDESC:Recent FDA food, drug, supplement, and medical device recalls from public openFDA enforcement data.
BEGIN:VEVENT
UID:D-0831-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Ramipril Capsules USP\, 10 mg\, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Ca...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0831-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0831-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1264-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Outshine Fruit Bars Strawberry\, 6-Count 2.5 ounce\, with UPC 041548610047\, packaged in pape...
DESCRIPTION:Class II Ongoing Firm: Dreyer'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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1264-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1264-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1265-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Outshine Fruit Bar Watermelon\, 6-Count 2.5 ounce with UPC 041548413624\, packaged in paper...
DESCRIPTION:Class II Ongoing Firm: Dreyer'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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1265-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1265-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1266-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Outshine Fruit Bars Grape\, 6-Count 2.5 ounce\, with UPC 041548244044\, packaged in paper out...
DESCRIPTION:Class II Ongoing Firm: Dreyer'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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1266-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1266-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1268-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Outshine Fruit Bars Black Cherry\, 6 Bars\, 2.5 ounce\, with UPC 041548000121\, packaged in pa...
DESCRIPTION:Class II Ongoing Firm: Dreyer'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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1268-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1268-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3035-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: POWERSEAL 5 MM (in diameter) 23 CM (long)\, Curved Jaw Sealer & Divider\, Double Action. GEI...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3035-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3035-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1271-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Marketside Tomato Bisque Soup Kit\, Tomato Bisque with Cheese Croutons & White Cheddar Chee...
DESCRIPTION: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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1271-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1271-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1278-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans n...
DESCRIPTION: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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1278-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1278-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0790-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Zicam\, Cold Remedy\, Medicated Nasal Swabs\, With Cooling Menthol & Eucalyptus\, 20 Single-Us...
DESCRIPTION:Class II Ongoing Firm: Church & 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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0790-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0790-2026%22
END:VEVENT
BEGIN:VEVENT
UID:N/A@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Clear glass bottle with black screw lid with multi label which reads in part as "***AFRICA...
DESCRIPTION: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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22N%2FA%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22N%2FA%22
END:VEVENT
BEGIN:VEVENT
UID:D-0775-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Levothyroxine Sodium Tablets\, USP\, 25 mcg (0.025 mg)\, 1000-count bottles\, Rx Only\, Manufac...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0775-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0775-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0776-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Levothyroxine Sodium Tablets\, USP\, 50 mcg (0.05 mg)\, 1000-count bottles\, Rx Only\, Manufact...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0776-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0776-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0777-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Levothyroxine Sodium Tablets\, USP\, 75 mcg (0.075 mg)\, 1000-count bottles\, Rx Only\, Manufac...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0777-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0777-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0781-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Levothyroxine Sodium Tablets\, USP\, 125 mcg (0.125 mg)\, 1000-count bottles\, Rx Only\, Manufa...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0781-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0781-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0782-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Levothyroxine Sodium Tablets\, USP\, 137 mcg (0.137 mg)\, packaged in a) 90-count bottles (ND...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0782-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0782-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0783-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Levothyroxine Sodium Tablets\, USP\, 150 mcg (0.15 mg)\, 1000-count bottles\, Rx Only\, Manufac...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0783-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0783-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0785-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Levothyroxine Sodium Tablets\, USP\, 200 mcg (0.2 mg)\, packaged in a) 90-count bottles (NDC...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0785-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0785-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0786-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Levothyroxine Sodium Tablets\, USP\, 300 mcg (0.3 mg)\, 90-count bottles\, Rx Only\, Manufactur...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0786-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0786-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0803-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Acthar Gel (repository corticotropin injection)\, 5 mL multiple-dose vial\, Rx Only\, Mfd. fo...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0803-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0803-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3033-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: ORT200\, operating room table\, including the ORT200 Covered Table Assembly\, Reconditioned\,...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3033-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3033-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3034-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: ORT300\, operating room table\, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3034-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3034-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1258-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net w...
DESCRIPTION:Class I Terminated Firm: H & 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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1258-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1258-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3014-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluo...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3014-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3014-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0789-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Drugs recall: Clobetasol Propionate Cream USP\, 0.05%\, 60 g tube\, Rx Only\, Manufactured for: Lupin Pharma...
DESCRIPTION: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 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0789-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0789-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1274-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling....
DESCRIPTION:Class II Ongoing Firm: Lidl US TRADING Reason: 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: Product was shipped to the following states: DC\, DE\, GA\, MD\, NJ\, NY\, NC\, PA\, SC\, & VA. Recall began: 2026-07-22 FDA IDs: H-1274-2026 / event 99493 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1274-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1274-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1275-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with cocon...
DESCRIPTION:Class II Ongoing Firm: Lidl US TRADING Reason: 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: Product was shipped to the following states: DC\, DE\, GA\, MD\, NJ\, NY\, NC\, PA\, SC\, & VA. Recall began: 2026-07-22 FDA IDs: H-1275-2026 / event 99493 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1275-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1275-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3004-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Merge PACS and Merge OrthoPACS\, medical imaging diagnostic workstation
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3004-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3004-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1259-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UP...
DESCRIPTION: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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1259-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1259-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2992-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Medline breathing circuits labeled as: 1) HUDSON RCI\, CIRCUIT\, HTD\, DL\, NEONATE\, 48\, Medli...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2992-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2992-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3022-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Medline convenience kits labeled as: 1) MAJOR PROCEDURE\, Medline Kit SKU CDS982040U\; 2) OP...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3022-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3022-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3026-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Medline convenience kits labeled as: 1) C-SECTION\, Medline Kit SKU DYNJ904612L\; 2) C-SECTI...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3026-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3026-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3028-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF\, Medline Kit SKU DYNJ54362...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3028-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3028-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3029-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Medline convenience kits labeled as: 1) LAMI FUSION\, Medline Kit SKU CDS982035Y\; 2) NON MB...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3029-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3029-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2994-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Medline medical convenience kits\, labeled as: 1) SINUS PACK-LF\, Medline Kit SKU DYNJ096614...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2994-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2994-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3017-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Devices recall: Fresenius Medical Care\, 2008T BlueStar Hemodialysis Machine\, Model Numbers: 191126\, 191130...
DESCRIPTION: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 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3017-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3017-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1263-2026@notyetneeded.com
DTSTAMP:20260907T223603Z
DTSTART;VALUE=DATE:20260902
DTEND;VALUE=DATE:20260903
SUMMARY:Food recall: Addall XR Shot 1 single bottle\, 2 fl. oz.\, liquid dietary supplement
DESCRIPTION: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 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1263-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1263-2026%22
END:VEVENT
END:VCALENDAR