Food Recall 2026 record Source: FDA
Eunha Fisheries Co., LTD
- Recall initiated
- July 1, 2026
- Reported by FDA
- August 12, 2026
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Food Recall 2026 record Source: FDA
Eunha Fisheries Co., LTD
- Recall initiated
- July 1, 2026
- Reported by FDA
- August 12, 2026
Food Recall 2026 record Source: FDA
Mellish Island Corp
- Recall initiated
- July 1, 2026
- Reported by FDA
- August 5, 2026
Drug Recall 2026 record Source: FDA
Dabigatran etexilate Capsules, 150 mg, 20-count carton (2x10), Rx only, Manufactured by: Alkem Laboratories, Mumbai, INDIA, Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7255-10.
- Recall initiated
- June 30, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
Dabigatran etexilate Capsules, 110 mg, 60-count carton (6x10), Rx Only, Manufactured by: Alkem Laboratories, Mumbai, INDIA, Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7254-68.
- Recall initiated
- June 30, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
Cinacalcet Hydrochloride Tablets, 90 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-412-02
- Recall initiated
- June 29, 2026
- Reported by FDA
- July 8, 2026
Drug Recall 2026 record Source: FDA
Cinacalcet Hydrochloride Tablets, 60 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-411-02
- Recall initiated
- June 29, 2026
- Reported by FDA
- July 8, 2026
Drug Recall 2026 record Source: FDA
Cinacalcet Hydrochloride Tablets, 30 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-410-02
- Recall initiated
- June 29, 2026
- Reported by FDA
- July 8, 2026
Drug Recall 2026 record Source: FDA
Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540, Made in India, NDC 69452-435-30.
- Recall initiated
- June 26, 2026
- Reported by FDA
- July 29, 2026
Food Recall 2026 record Source: FDA
Total Nutrition Inc
- Recall initiated
- June 26, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, Rx Only, 100 capsules, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC: 0527-0790-37.
- Recall initiated
- June 26, 2026
- Reported by FDA
- July 8, 2026
Food Recall 2026 record Source: FDA
GELLERT GLOBAL GROUP
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED BY: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785.
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 22, 2026
Drug Recall 2026 record Source: FDA
meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41250-835-33, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544.
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 22, 2026
Drug Recall 2026 record Source: FDA
Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 22, 2026
Drug Recall 2026 record Source: FDA
LEADER, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit -1 RUBBER BULB SYRINGE, 0.5 FL OZ DROPS, (NDC 70000-0689-1); b) 1 bottle (NDC 70000-0688-1), DIST. BY CARDINAL HEALTH, DUBLIN, OH 43017.
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 22, 2026
Drug Recall 2026 record Source: FDA
GOOD NEIGHBOR PHARMACY, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit - Washer Bulb Included, (NDC 46122-556-05); b) 1 bottle (NDC 46122-557-05), Distributed by: AmerisourceBergen, 1 West First Avenue, Conshohocken, PA 19428.
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 22, 2026
Drug Recall 2026 record Source: FDA
FAMILY Wellness, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), Kit - Washer Bulb Included, (NDC 55319-835-01), DISTRIBUTED BY: MIDWOOD BRANDS LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320.
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 22, 2026
Drug Recall 2026 record Source: FDA
AUDIOLOGIST'S CHOICE, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL) a) Kit - Washer Bulb Included (NDC 59256-001-02); b) 1 bottle (NDC 59256-836-34), Distributed By: Oaktree Products Inc., St. Louis. MO 63005.
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 22, 2026
Drug Recall 2026 record Source: FDA
TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS INCLUDED (NDC 36800-835-33); b) 1 bottle (NDC 36800-835-34), DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007.
- Recall initiated
- June 25, 2026
- Reported by FDA
- July 22, 2026
Data last updated:
Investigations and recalls may be ongoing; status, case counts, and guidance are updated by the source agency as events continue. Read the full medical disclaimer.
