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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 101–120 of 224 alerts

Drug Recall 2026 record Source: FDA

QC Quality Choice, Carbamide Peroxide, 6.5%, 0.5 FL. OZ. (15 mL) a) Washer Bulb included (NDC 63868-026-15); b) 1 bottle (NDC 63868-027-16), Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376.

Recall initiated
June 25, 2026
Reported by FDA
July 22, 2026

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Drug Recall 2026 record Source: FDA

Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%, 0.5 fl. oz. (15 mL); b) 1 bottle of Clinere Carbamide Peroxide (0,50 fl. oz. (15 mL), Dist. by: Quest Products LLC, Pleasant Prairie, WI 53158, NDC 68229-102-01.

Recall initiated
June 25, 2026
Reported by FDA
July 22, 2026

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Drug Recall 2026 record Source: FDA

CVS Health, Carbamide Peroxide, 6.5%, 0.5 FL Oz (15 mL), a) Bottle (NDC 51316-822-00.); b) Kit (1 BULB, Syringe & Drops- NDC 51316-823-00.), Distributed by: CVS Pharmacy., Inc. One CVS Drive, Woonsocket, RI 02895,

Recall initiated
June 25, 2026
Reported by FDA
July 22, 2026

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Drug Recall 2026 record Source: FDA

Cetirizine Hydrochloride Tablets USP 5 mg, 100-count bottle, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of J.B. Chemicals & Pharmaceuticals, Ltd.), Mumbai 400 030, India. Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 16571-401-10.

Recall initiated
June 24, 2026
Reported by FDA
July 29, 2026

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Drug Recall 2026 record Source: FDA

Azacitidine for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For Subcutaneous and Intravenous Use, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0857-01

Recall initiated
June 24, 2026
Reported by FDA
July 15, 2026

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Drug Recall 2026 record Source: FDA

Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01

Recall initiated
June 24, 2026
Reported by FDA
July 15, 2026

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Drug Recall 2026 record Source: FDA

Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01

Recall initiated
June 24, 2026
Reported by FDA
July 15, 2026

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Drug Recall 2026 record Source: FDA

Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0834-01

Recall initiated
June 24, 2026
Reported by FDA
July 15, 2026

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Drug Recall 2026 record Source: FDA

Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park One Dr, Suite 100, Sugar Land, TX 77478, Product code: 70092-1310-46.

Recall initiated
June 24, 2026
Reported by FDA
July 15, 2026

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Food Recall 2026 record Source: FDA

Lehi Valley Trading Company, Inc

Recall initiated
June 24, 2026
Reported by FDA
July 15, 2026

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Food Recall 2026 record Source: FDA

Trafa Pharmaceutical Inc.

Recall initiated
June 24, 2026
Reported by FDA
July 15, 2026

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Drug Recall 2026 record Source: FDA

Nystatin Cream USP, (100,000 USP Nystatin Units), NET WT 15 g, Rx only, 15 g tube, Manufactured by Padagis, Yeruham, Israel, NDC 45802-059-35

Recall initiated
June 23, 2026
Reported by FDA
July 22, 2026

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Drug Recall 2026 record Source: FDA

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur - 441108, INDIA, NDC 70748-311-01

Recall initiated
June 23, 2026
Reported by FDA
July 8, 2026

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Food Recall 2026 record Source: FDA

General Mills James Ford Bell Technical Center

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

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Food Recall 2026 record Source: FDA

General Mills James Ford Bell Technical Center

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

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Food Recall 2026 record Source: FDA

Provision Health Corp. dba PH Labs

Recall initiated
June 18, 2026
Reported by FDA
July 8, 2026

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Food Recall 2026 record Source: FDA

Provision Health Corp. dba PH Labs

Recall initiated
June 18, 2026
Reported by FDA
July 8, 2026

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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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