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Health Alerts

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 1–20 of 242 alerts

Food Recall 2026 record Source: FDA

Galil Importing Corp

Recall initiated
September 24, 2026
Reported by FDA
October 7, 2026

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Drug Recall 2026 record Source: FDA

Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-1318-3

Recall initiated
September 23, 2026
Reported by FDA
October 7, 2026

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Drug Recall 2026 record Source: FDA

FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per vial, STERILE, Manufactured for: Covalent Management, Inc., Manassas, VA 20109. NDC: 82724-007-19

Recall initiated
September 17, 2026
Reported by FDA
October 7, 2026

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Drug Recall 2026 record Source: FDA

Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottle, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807. NDC: 27241-126-02

Recall initiated
September 17, 2026
Reported by FDA
October 7, 2026

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Drug Recall 2026 record Source: FDA

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) with Hang Tag, 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15

Recall initiated
September 15, 2026
Reported by FDA
September 30, 2026

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Drug Recall 2026 record Source: FDA

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15

Recall initiated
September 15, 2026
Reported by FDA
September 30, 2026

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Food Recall 2026 record Source: FDA

WWF Operating Company

Recall initiated
September 15, 2026
Reported by FDA
September 30, 2026

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Food Recall 2026 record Source: FDA

Pacific Health Sciences Llc

Recall initiated
September 14, 2026
Reported by FDA
October 7, 2026

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Food Recall 2026 record Source: FDA

TODD'S SEEDS LLC

Recall initiated
September 11, 2026
Reported by FDA
October 7, 2026

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Food Recall 2026 record Source: FDA

TODD'S SEEDS LLC

Recall initiated
September 11, 2026
Reported by FDA
October 7, 2026

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Food Recall 2026 record Source: FDA

TODD'S SEEDS LLC

Recall initiated
September 11, 2026
Reported by FDA
October 7, 2026

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Food Recall 2026 record Source: FDA

TODD'S SEEDS LLC

Recall initiated
September 11, 2026
Reported by FDA
October 7, 2026

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Food Recall 2026 record Source: FDA

TODD'S SEEDS LLC

Recall initiated
September 11, 2026
Reported by FDA
October 7, 2026

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Food Recall 2026 record Source: FDA

TODD'S SEEDS LLC

Recall initiated
September 11, 2026
Reported by FDA
October 7, 2026

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Drug Recall 2026 record Source: FDA

Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA, Malvern, PA, NDC 42023-179-05

Recall initiated
September 8, 2026
Reported by FDA
October 7, 2026

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Drug Recall 2026 record Source: FDA

Estradiol Gel, 0.1%, 0.25 mg, 30-packets per carton, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08907, NDC 69238-2452-3.

Recall initiated
September 8, 2026
Reported by FDA
October 7, 2026

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Food Recall 2026 record Source: FDA

WFM Purchasing, LP

Recall initiated
September 8, 2026
Reported by FDA
September 30, 2026

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Food Recall 2026 record Source: FDA

Kwok Shing, Inc.

Recall initiated
September 8, 2026
Reported by FDA
September 30, 2026

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Food Recall 2026 record Source: FDA

Evergreen Fresh Sprouts LLC

Recall initiated
September 4, 2026
Reported by FDA
September 30, 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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