Food Recall 2026 record Source: FDA
Tiffany Food Corp
- Recall initiated
- August 28, 2026
- Reported by FDA
- September 23, 2026
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Food Recall 2026 record Source: FDA
Frutas y Hortalizas del Sur S.A.
- Recall initiated
- August 28, 2026
- Reported by FDA
- September 23, 2026
Drug Recall 2026 record Source: FDA
Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ, 08540; Manufactured by: Macleods Pharmaceuticals, Ltd, Baddi, Himachal Pradesh, INDIA, NDC 33342-068-07.
- Recall initiated
- August 27, 2026
- Reported by FDA
- September 30, 2026
Food Recall 2026 record Source: FDA
FOODS ALIVE INC.
- Recall initiated
- August 26, 2026
- Reported by FDA
- September 23, 2026
Drug Recall 2026 record Source: FDA
Carton label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, 4 Single Dose Vials, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505, Made in India, NDC 67457-386-81. Vial Label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, Single Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505, Made in India, NDC 67457-386-00.
- Recall initiated
- August 26, 2026
- Reported by FDA
- September 9, 2026
Food Recall 2026 record Source: FDA
Optimus Inc. d/b/a/ Markys Caviar
- Recall initiated
- August 25, 2026
- Reported by FDA
- September 23, 2026
Food Recall 2026 record Source: FDA
Quality Dairy Farms Inc.
- Recall initiated
- August 25, 2026
- Reported by FDA
- September 23, 2026
Drug Recall 2026 record Source: FDA
Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-255-01.
- Recall initiated
- August 25, 2026
- Reported by FDA
- September 16, 2026
Drug Recall 2026 record Source: FDA
Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-732-10
- Recall initiated
- August 24, 2026
- Reported by FDA
- September 16, 2026
Drug Recall 2026 record Source: FDA
traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o, Zagreb, Croatia, Manufactured For: Teva Pharmaceuticals, Parsippany, NJ 07054, NDC 50111-560-01
- Recall initiated
- August 24, 2026
- Reported by FDA
- September 9, 2026
Drug Recall 2026 record Source: FDA
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.
- Recall initiated
- August 24, 2026
- Reported by FDA
- September 2, 2026
Food Recall 2026 record Source: FDA
International Sprout Holdings, Inc
- Recall initiated
- August 23, 2026
- Reported by FDA
- September 16, 2026
Food Recall 2026 record Source: FDA
Everything Sprouts, LLC
- Recall initiated
- August 22, 2026
- Reported by FDA
- September 23, 2026
Food Recall 2026 record Source: FDA
Everything Sprouts, LLC
- Recall initiated
- August 22, 2026
- Reported by FDA
- September 23, 2026
Food Recall 2026 record Source: FDA
Everything Sprouts, LLC
- Recall initiated
- August 22, 2026
- Reported by FDA
- September 23, 2026
Food Recall 2026 record Source: FDA
Everything Sprouts, LLC
- Recall initiated
- August 22, 2026
- Reported by FDA
- September 23, 2026
Drug Recall 2026 record Source: FDA
Thyroid Tablets, USP, 1/2 Grain (30 mg), Each tablet contains: levothyroxine (T4) 19 mcg, liothyronine (T3) 4.5 mcg, 100 Tablets, Rx only, Distributed by: Vitruvias Therapeutics, Auburn, AL 36830, Product of USA, NDC 69680-166-00.
- Recall initiated
- August 21, 2026
- Reported by FDA
- September 23, 2026
Drug Recall 2026 record Source: FDA
Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC: 51407-445-30.
- Recall initiated
- August 21, 2026
- Reported by FDA
- September 9, 2026
Drug Recall 2026 record Source: FDA
Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 3000mg, HempSeed Oil 2000mg),4 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-6; UPC 8 50041 64004 4
- Recall initiated
- August 21, 2026
- Reported by FDA
- September 9, 2026
Drug Recall 2026 record Source: FDA
Broadway Joe's Pain Cream, (Histamine Dihydrochloride 0.025%), 1500mg CBD Isolate, 1000mg Hempseed oil, 2 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-5, UPC 8 50041 64003 7
- Recall initiated
- August 21, 2026
- Reported by FDA
- September 9, 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.
