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FDA · Drugs ·

Cefazolin in Dextrose recall

Baxter Healthcare Corporation recalled Cefazolin in Dextrose on August 19, 2026 because of presence of Particulate Matter. It was sold nationwide.

Why it was recalled

Presence of Particulate Matter

What's recalled

Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic Container, Frozen Premix, Sterile, Rx only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-3508-41.

Quantity: 19,032 bags

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Baxter Healthcare Corporation, Deerfield, IL
Date
Severity
Class I · most serious
the most serious: the product could cause serious health problems or death.
Where sold
Nationwide
US Nationwide.
Status
Ongoing
Recall number
D-0787-2026
Source
U.S. Food and Drug Administration

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