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Class I · Most seriousActive recall

Cefazolin

A reasonable chance it could cause serious harm or death.

Does this affect you?
Check your lot numberLot # LD175708, Exp Date: 14-Feb-2027.
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Particulate Matter

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byBaxter Healthcare Corporation, Deerfield, IL 60015, USA
Brand nameCEFAZOLIN
Generic nameCEFAZOLIN SODIUM
Active ingredient(s)CEFAZOLIN SODIUM
Distributed by / forBaxter Healthcare Corporation
NDC0338-3508-41
Show the full FDA record
Full product labelCefazolin 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.
Recalling firmBaxter Healthcare Corporation
DistributionUS Nationwide.
Quantity19,032 bags
Recall initiated2026-07-24
Report date2026-08-19
Recall completed—
Recall numberD-0787-2026
ClassificationClass I
FDA statusOngoing
Origin on fileDeerfield IL United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.