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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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Showing 81–100 of 1,205 alerts

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

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Food Recall 2026 record Source: FDA

Optimus Inc. d/b/a/ Markys Caviar

Recall initiated
August 25, 2026
Reported by FDA
September 23, 2026

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Food Recall 2026 record Source: FDA

Quality Dairy Farms Inc.

Recall initiated
August 25, 2026
Reported by FDA
September 23, 2026

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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

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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

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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

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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

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Food Recall 2026 record Source: FDA

International Sprout Holdings, Inc

Recall initiated
August 23, 2026
Reported by FDA
September 16, 2026

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Food Recall 2026 record Source: FDA

Everything Sprouts, LLC

Recall initiated
August 22, 2026
Reported by FDA
September 23, 2026

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Food Recall 2026 record Source: FDA

Everything Sprouts, LLC

Recall initiated
August 22, 2026
Reported by FDA
September 23, 2026

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Food Recall 2026 record Source: FDA

Everything Sprouts, LLC

Recall initiated
August 22, 2026
Reported by FDA
September 23, 2026

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Food Recall 2026 record Source: FDA

Everything Sprouts, LLC

Recall initiated
August 22, 2026
Reported by FDA
September 23, 2026

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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.

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