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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 423 alerts

Drug Recall 2026 record Source: FDA

Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India, NDC 59651-719-99

Recall initiated
July 23, 2026
Reported by FDA
August 12, 2026

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Drug Recall 2026 record Source: FDA

Azelaic Acid Gel, 15%, 50 gram tubes, For Topical Use only, Rx only, Distributed by: Glenmark Pharmaceuticals Inc., USA, Elmwood Park, NJ 07407, NDC 68462-626-52.

Recall initiated
July 23, 2026
Reported by FDA
August 5, 2026

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Food Recall 2026 record Source: FDA

MIDWEST POULTRY SERVC C/O H & LELECTRIC

Recall initiated
July 22, 2026
Reported by FDA
August 19, 2026

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Food Recall 2026 record Source: FDA

MIDWEST POULTRY SERVC C/O H & LELECTRIC

Recall initiated
July 22, 2026
Reported by FDA
August 19, 2026

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Drug Recall 2026 record Source: FDA

Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro Labs Limited, India, Manufactured for: Micro Labs USA Inc., Somerset, NJ 08873. NDC 42571-147-26.

Recall initiated
July 22, 2026
Reported by FDA
August 5, 2026

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CDC Announcement 2026 record Source: CDC

Salmonella Outbreak Linked to Shell Eggs

Start date
July 22, 2026
Last updated

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Drug Recall 2026 record Source: FDA

Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1

Recall initiated
July 17, 2026
Reported by FDA
August 12, 2026

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Drug Recall 2026 record Source: FDA

Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1

Recall initiated
July 17, 2026
Reported by FDA
August 12, 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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