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Class IOngoing

Cefazolin in Dextrose recall

FDA recall D-0787-2026 · initiated Jul 24, 2026

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Aug 19, 2026How we research

Baxter Healthcare Corporation recalled Cefazolin in Dextrose in Jul 2026 — an FDA Class I recall (D-0787-2026) because Presence of Particulate Matter.

Most serious — a reasonable probability that use will cause serious harm or death.

Why it was recalled

Presence of Particulate Matter

Something got into the product

A physical or chemical contaminant was found — glass or metal fragments, or a solvent that should not be there.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot # LD175708, Exp Date: 14-Feb-2027.

Quantity recalled: 19,032 bags

Details

Product
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.
Recalling company
Baxter Healthcare Corporation
Classification
Class I
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
US Nationwide.
Initiated
Jul 24, 2026
FDA report date
Aug 19, 2026
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Cefazolin in Dextrose recalled?
Baxter Healthcare Corporation recalled Cefazolin in Dextrose in Jul 2026 — an FDA Class I recall (D-0787-2026) because Presence of Particulate Matter. Most serious — a reasonable probability that use will cause serious harm or death.
Why was Cefazolin in Dextrose recalled?
Per the FDA enforcement record, the reason for recall D-0787-2026 was: Presence of Particulate Matter
Is a recalled Cefazolin in Dextrose dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Cefazolin in Dextrose are affected?
Distributed: US Nationwide.. The recall covers these lots — Lot # LD175708, Exp Date: 14-Feb-2027.. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0787-2026.

Source: openFDA Drug Enforcement record D-0787-2026 ↗

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