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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 261–280 of 441 alerts

Food Recall 2026 record Source: FDA

Prospector Popcorn, LLC

Recall initiated
July 15, 2026
Reported by FDA
August 26, 2026

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Food Recall 2026 record Source: FDA

Prospector Popcorn, LLC

Recall initiated
July 15, 2026
Reported by FDA
August 26, 2026

View Details

Food Recall 2026 record Source: FDA

Prospector Popcorn, LLC

Recall initiated
July 15, 2026
Reported by FDA
August 26, 2026

View Details

Food Recall 2026 record Source: FDA

Prospector Popcorn, LLC

Recall initiated
July 15, 2026
Reported by FDA
August 26, 2026

View Details

FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE

Glutinous Rice Balls with Black Sesame Filling and Black & White Glutinous Rice Balls with Black Sesame Filling

Announced by FDA
July 15, 2026

View FDA Announcement

Drug Recall 2026 record Source: FDA

Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc, S. Beloil, IL 61080, unit-dose oral syringes, NDCs 68094-073-01 (oral syringe) and 68094-073-58 (case).

Recall initiated
July 14, 2026
Reported by FDA
July 29, 2026

View Details

Drug Recall 2026 record Source: FDA

Rohto Cooling Eye Drops Cool Relief (naphazoline hydrochloride 0.012%, polysorbate 80 0.2%), Sterile, 0.4 FL OZ (13 mL) each, Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742010749, NDC 10742-8141-1

Recall initiated
July 14, 2026
Reported by FDA
July 29, 2026

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Food Recall 2026 record Source: FDA

PT Organics Limited

Recall initiated
July 13, 2026
Reported by FDA
August 12, 2026

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Drug Recall 2026 record Source: FDA

Rising, Cyproheptadine Hydrochloride Syrup, 2mg/5 mL, 473 mL (ONE PINT), Rx only, Manufactured for: Rising Pharma Holdings, Inc., East Brunswick, NJ, Manufactured by: Lyne Laboratories, Inc., Brockton, MA. NDC 64980-504-48.

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

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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

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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

View Details

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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