Cefazolin in Dextrose
Presence of Particulate Matter
Yes — there is an active recall. 3 ongoing FDA recalls mention Cefazolin (36 total). Check the affected lots below.
Most common reason: Sterility / contamination (27 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Cefazolin. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Presence of Particulate Matter
Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were found to contain vials labeled as penicillin G potassium for Injection, USP, 20 million Unit. The vials contained Cefozalin
Lack of assurance of sterility.
Lack of sterility assurance
Lack of sterility assurance
cGMP deviations: Temperature abuse
cGMP deviations: Temperature abuse
Lack of sterility assurance.
Lack of sterility assurance.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lack of sterility assurance.
Lack of sterility assurance.
Lack of sterility assurance.
Lack of Assurance of Sterility: Potential leakage of bags.
Lack of sterility assurance.
Lack of Assurance of Sterility: Product made with recalled 0.9% sodium chloride bags which have the potential to leak.
Lack of assurance of sterility: Product bags leaking at seam.
Lack of assurance of sterility: Product bags leaking at seam.
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Sterility Assurance
Lack of Assurance of Sterility
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