Food Recall 2026 record Source: FDA
Green Jeeva LLC
- Recall initiated
- July 8, 2026
- Reported by FDA
- July 29, 2026
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FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Pounded Yam
- Announced by FDA
- July 7, 2026
Drug Recall 2026 record Source: FDA
Trokendi XR, topiramate extended-release capsules, 25mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA, NDC 17772-101-30.
- Recall initiated
- July 6, 2026
- Reported by FDA
- July 29, 2026
Drug Recall 2026 record Source: FDA
CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials, Rx Only, Manufactured for: Chiesi USA, Inc., Cary, NC 27518, by Fresenius Kabi, Graz, Austria, NDC 10122-611-10.
- Recall initiated
- July 6, 2026
- Reported by FDA
- July 22, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Organic IQF Frozen Blueberries 10 oz
- Announced by FDA
- July 6, 2026
Food Recall 2026 record Source: FDA
Frutas y Hortalizas del Sur S.A.
- Recall initiated
- July 3, 2026
- Reported by FDA
- July 22, 2026
Drug Recall 2026 record Source: FDA
Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India, NDC 67457-386-00.
- Recall initiated
- July 2, 2026
- Reported by FDA
- August 5, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
High Protein Chopped Chicken & Duck Flavor Wet Dog Food
- Announced by FDA
- July 2, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Kimchi & Tofu Kimbap
- Announced by FDA
- July 2, 2026
Drug Recall 2026 record Source: FDA
Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VMC.
- Recall initiated
- July 1, 2026
- Reported by FDA
- August 19, 2026
Food Recall 2026 record Source: FDA
JINA F&C
- Recall initiated
- July 1, 2026
- Reported by FDA
- August 12, 2026
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
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
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Sliced Korean Halibut and Flounder Sashimi products
- Announced by FDA
- July 1, 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
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.
