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Your unified view of current, active outbreak investigations, elevated disease activity, and food and drug recalls -- reported directly by CDC, FDA, and USDA. Not CDC NORS, which is a historical archive compiled well after an investigation closes (see Data Explorer for the full historical record).

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Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distributed by Cardinal Health, Dublin, OH 43017. NDC Carton: 55154-3558-0; NDC Blister: 0904-6949-61

Recall initiated: July 13, 2026
Reported by FDA: July 29, 2026

Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6956-61

Recall initiated: July 13, 2026
Reported by FDA: July 29, 2026

Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6955-61

Recall initiated: July 13, 2026
Reported by FDA: July 29, 2026

Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 112 mcg (0.0112 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6954-61

Recall initiated: July 13, 2026
Reported by FDA: July 29, 2026

Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6952-61

Recall initiated: July 13, 2026
Reported by FDA: July 29, 2026

Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6951-61

Recall initiated: July 13, 2026
Reported by FDA: July 29, 2026

Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6950-61

Recall initiated: July 13, 2026
Reported by FDA: July 29, 2026

Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6949-61

Recall initiated: July 13, 2026
Reported by FDA: July 29, 2026

Food Recall 2026 record Source: FDA

Pack'n Fresh LLC

Recall initiated: July 9, 2026
Reported by FDA: August 12, 2026

Drug Recall 2026 record Source: FDA

BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0.03fl oz (1 mL) each, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31

Recall initiated: July 9, 2026
Reported by FDA: July 22, 2026

Drug Recall 2026 record Source: FDA

Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC., Parsnippany, NJ 07054. NDC: 67877-500-30

Recall initiated: July 8, 2026
Reported by FDA: July 29, 2026

Food Recall 2026 record Source: FDA

Man Fon, Inc.

Recall initiated: July 8, 2026
Reported by FDA: July 29, 2026

Food Recall 2026 record Source: FDA

Man Fon, Inc.

Recall initiated: July 8, 2026
Reported by FDA: July 29, 2026

Food Recall 2026 record Source: FDA

Green Jeeva LLC

Recall initiated: July 8, 2026
Reported by FDA: July 29, 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

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

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

Data last updated: September 5, 2026 ET

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.

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