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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 441 alerts

Drug Recall 2026 record Source: FDA

Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0718-12.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Vancomycin Injection, USP, in 0.9% Sodium Chloride, 1g per 200 mL (5 mg/mL) in GALAXY Single-Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL, 60015 USA, NDC 0338-3583-01.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Vasopressin, in 0.9% Sodium Chloride Injection, 40 units per 100 mL (0.4 units/mL), 100mL Single-Dose Container, Rx only, Sterile, Baxter Healthcare Corporation, Deerfield, IL, 60015 USA, NDC 0338-9647-12.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL (18 mg/mL), in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Manufactured by: Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 43066-995-24.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL (18 mg/mL), in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Manufactured by: Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-4114-50.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Clindamycin Phosphate in 0.9% Sodium Chloride Injection, 600 mg per 50 mL (12 mg/mL), 50 mL Single-Dose GALAXY Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-9549-50.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-3814-50.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Nexterone (amiodarone HCI), 360 mg/200 mL (1.8 mg/mL) in GALAXY Single-Dose Container, sterile, Nonpyrogenic, iso-osmotic solution in Dextrose, Baxter Healthcare Corporation, Deerfield, IL 60015, Made in the USA, NDC 43066-360-20.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection, 40 mg in 200 mL (0.2 mg/mL) in GALAXY Single-Dose Container, Manufactured and Marketed by: Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 43066-016-10.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Pantoprazole Sodium in 0.9% Sodium Chloride Injection, 80 mg/100 mL (0.8 mg/mL) Single-Dose Infusion Bag in 100 mL GALAXY Container, Rx only, Sterile, Baxter Healthcare Corporation, Deerfield, IL, 60015, USA, NDC 0338-9648-12.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), 100mL Single-Dose Container, Rx only, Sterile, Baxter Healthcare Corporation, Deerfield, IL, 60012 USA, NDC 0338-9640-12.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-9557-12.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Famotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single Dose Container, Rx Only, Sterile Nonpyrogenic, Baxter International Inc., Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-5197-41.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Clindamycin Injection USP in 5% Dextrose, 600 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-3612-50.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Daptomycin, in 0.9% Sodium Chloride Injection, 500 mg per 50 mL (10 mg/mL), 500 mg total, in 50 mL Single Dose Container (24 bags/carton), Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0714-24.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

MYXREDLIN, Insulin Human in 0.9% Sodium Chloride Injection, 100 units/100 mL (1 unit/mL), Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0126-12.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Drug Recall 2026 record Source: FDA

Vancomycin Injection, USP in 5% Dextrose, 1 g per 200mL (5 mg/mL), in GALAXY Single-Dose Container, Rx only, Sterile Nonpyrogenic, Iso-osmotic, Baxter Healthcare Corporation, Deerfield, IL, 60015 USA, NDC 0338-3552-48.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Food Recall 2026 record Source: FDA

WEIS MARKETS, INC.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Food Recall 2026 record Source: FDA

Ron's Home Style Foods, Inc.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 2026

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Food Recall 2026 record Source: FDA

Ron's Home Style Foods, Inc.

Recall initiated
August 6, 2026
Reported by FDA
September 9, 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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