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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 321–340 of 1,237 alerts

Drug Recall 2026 record Source: FDA

Atropine Sulfate injection, USP, 1 mg/mL, For intravenous Use, Sterile, packaged in a) 1 mL Single-Dose Vial (NDC 0517-1001-01), and b) 25x1 mL Single-Dose Vial (NDC 0517-1001-25), Rx only, AMERICAN REGENT INC., SHIRLEY, NY 11967.

Recall initiated
July 24, 2026
Reported by FDA
August 26, 2026

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Drug Recall 2026 record Source: FDA

AMINAOCAPROIC ACID INJECTION, USP, 250 mg/mL (5 g/20 mL), packaged in a) 20 mL MULTIPLE DOSE VIAL FOR IV INFUSION (NDC 0517-9120-01), and b) 25x20 mL MULTIPLE DOSE VIALS (NDC 0517-9120-25), Rx Only, American Regent, Inc., Shirley, NY 11967.

Recall initiated
July 24, 2026
Reported by FDA
August 26, 2026

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Drug Recall 2026 record Source: FDA

Cyanocobalamin injection USP, 10,000 mcg/10 mL (1,000 mcg/mL), For IM or SC Use Only, packaged in a) 10 mL Multi-Dose Vial (NDC 0517-0032-01) and b) 25x10 mL Multi-Dose Vials (NDC 0517-0032-25), Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.

Recall initiated
July 24, 2026
Reported by FDA
August 26, 2026

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Drug Recall 2026 record Source: FDA

Cyanocobalamin injection USP, 1,000 mcg/mL, For IM or SC Use Only, packaged in a) 1 mL Multi-Dose Vial (NDC 0517-0031-01), and b) 25x1 mL Multi-Dose Vials (NDC 0517-0031-25) Rx only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.

Recall initiated
July 24, 2026
Reported by FDA
August 26, 2026

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Drug Recall 2026 record Source: FDA

Nitroglycerin injection, USP, 50 mg/10 mL (5 mg/mL), packaged in a) 10 mL vials (NDC 0517-4810-01), b) 25x10mL vials (NDC 0517-4810-25) RX only, AMERICAN REGENT, INC., Shirley, NY 11967.

Recall initiated
July 24, 2026
Reported by FDA
August 26, 2026

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Drug Recall 2026 record Source: FDA

Acamprosate Calcium, Delayed-Release Tablets, 333 mg, 180 tablets bottles, Rx only, Mylan Pharmaceuticals Inc., Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 266505, NDC 0378-6333-80.

Recall initiated
July 24, 2026
Reported by FDA
August 26, 2026

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Active Investigation 2026 record Source: FDA

Cyclosporiasis

Cases
240
Start date
July 22, 2026
Last updated

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Active Investigation 2026 record Source: FDA

Listeria monocytogenes

Cases
11
Start date
July 22, 2026
Last updated

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Food Recall 2026 record Source: FDA

Coast Citrus Distributors

Recall initiated
July 22, 2026
Reported by FDA
August 26, 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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Active Investigation 2026 record Source: FDA

Salmonella Javiana

Start date
July 22, 2026
Last updated

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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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