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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 221–240 of 424 alerts

Drug Recall 2026 record Source: FDA

BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 100 x 3 mL applicators/case, NDC 54365-400-33, calatog 930415NS: b) 250 x 3mL applicators/case, bulk catalog number 930415NSB; STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co.

Recall initiated
June 11, 2026
Reported by FDA
July 8, 2026

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Drug Recall 2026 record Source: FDA

ChloraPrep FREPP, Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) 500 x 1.5 mL applicators/case, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-30, Catalog number 930599NSB

Recall initiated
June 11, 2026
Reported by FDA
July 8, 2026

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Drug Recall 2026 record Source: FDA

BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG), and 70% v/v isopropyl alcohol (IPA), Packaged as a) 100 x 3ml applicators/case, NDC 54365-400-32, catalog 930400NS; b) 250 x 3ml applicators/case, NDC 54365-400-32, bulk Catalog 930500NSB, Sterile Solution, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co.

Recall initiated
June 11, 2026
Reported by FDA
July 8, 2026

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Drug Recall 2026 record Source: FDA

BD PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w), 50 x 26 mL Applicator/case, STERILE SOLUTION, CAREFUSION 213, LLC, EL PASO, TX 79912, subsidiary of Beckton, Dickson and Co, Catalog Number 960120NSB; NDC 54365-014-42.

Recall initiated
June 11, 2026
Reported by FDA
July 8, 2026

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Drug Recall 2026 record Source: FDA

BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), packaged as a) 100 x 10.5 mL applicators/case, NDC 54365-400-35, Catalog Number: 930715NS; b) 100 x 10.5 mL applicators/case, Catalog Number bulk 930715NSB, NDC 54365-400-35; STERILE SOLUTION, CAREFUSION 213, LLC, EL PASO, TX 79912, subsidiary of Beckton, Dickson and Co.

Recall initiated
June 11, 2026
Reported by FDA
July 8, 2026

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

TNVitamins Ultra Potent Complete Green Superfood Capsules and Doctor’s Pride Complete Green Superfood capsules

Announced by FDA
June 11, 2026

View FDA Announcement

Drug Recall 2026 record Source: FDA

Gemcitabine Injection, 1 g per 26.3 mL (38 mg/mL), 26.3 mL Single-Dose Vial, For Intravenous Infusion ONLY, Rx only, Manufactured by: THYMOORGAN PHARMAZIE GmbH, Schiffgraben 23, 38690 Goslar, Germany; Distributed by: Hikma, Berkeley Heights, NJ 07922. NDC: 0143-9341-01

Recall initiated
June 10, 2026
Reported by FDA
July 8, 2026

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Drug Recall 2026 record Source: FDA

IMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single dose vial, Manufactured by Accord BioPharma Inc., 8041 Arco corporate Drive, Suite 200, Raleigh, NC 27617, USA, Manufactured at: Catalent Indiana, LLC, 1300 S. Patterson Drive, Bloomington, IN 47403, USA, NDC 69448-019-26.

Recall initiated
June 10, 2026
Reported by FDA
July 8, 2026

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Drug Recall 2026 record Source: FDA

Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Distributed by Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 85766-187-01.

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

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Drug Recall 2026 record Source: FDA

Accucaine, Kit contains: Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Distributed by Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 76420-715-01.

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

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Drug Recall 2026 record Source: FDA

Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: lntas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-458-15.

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

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Drug Recall 2026 record Source: FDA

Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured by: OneSource Specialty, Pharma Limited, Bengaluru - 561 203, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-893-31

Recall initiated
June 7, 2026
Reported by FDA
July 15, 2026

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Food Recall 2026 record Source: FDA

Nelson & Isa Lacteos LLC

Recall initiated
June 5, 2026
Reported by FDA
August 5, 2026

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

Pearl Milling Company Original Pancake & Waffles Complete – 5.99 oz (170g)

Announced by FDA
June 5, 2026

View FDA Announcement

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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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