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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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Drug Recall 2026 record Source: FDA

CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-603-51

Recall initiated: July 30, 2026
Reported by FDA: August 19, 2026

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

Aquafaba Powder 4oz (113g) and (12 oz (340g) flexible foil pouches

Announced by FDA: July 30, 2026

View FDA Announcement

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

Organic IQF Frozen Blueberries and Whole Mixed Berries, 10 oz and 48 oz

Announced by FDA: July 30, 2026

Terminated

View FDA Announcement

Drug Recall 2026 record Source: FDA

PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgewater, NY 08807. NDC: 70121-2461-1

Recall initiated: July 29, 2026
Reported by FDA: August 26, 2026

Drug Recall 2026 record Source: FDA

PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgewater, NY 08807. NDC: 70121-2453-1

Recall initiated: July 29, 2026
Reported by FDA: August 26, 2026

Drug Recall 2026 record Source: FDA

CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-724-04.

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.NDC 71170-712-03

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Drug Recall 2026 record Source: FDA

SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05

Recall initiated: July 29, 2026
Reported by FDA: August 19, 2026

Food Recall 2026 record Source: FDA

Kerry, Inc

Recall initiated: July 29, 2026
Reported by FDA: August 12, 2026

Food Recall 2026 record Source: FDA

Wonton Specialists

Recall initiated: July 28, 2026
Reported by FDA: September 9, 2026

Food Recall 2026 record Source: FDA

Wonton Specialists

Recall initiated: July 28, 2026
Reported by FDA: September 9, 2026

Data last updated: September 20, 2026 ET

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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