Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic Container
Summary
The FDA issued a recall for Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusi by Baxter Healthcare Corporation. Reason: Presence of Particulate Matter.
Details
Source
Drug Recall
External ID
4c81b3a9-81ee-4bed-bfb3-1300b7ef3299
Action Date
2026-08-19
Status
Ongoing
Category
drug
Product Description
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.
Lot/Code Info: Lot # LD175708, Exp Date: 14-Feb-2027.
Reason for Recall
Presence of Particulate Matter
Distribution
US Nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-24
Company
Deerfield, IL
Context & Analysis
This is a unclassified recall.
This was one of 28 drug recalls issued in the same week, part of 68 drug-related FDA actions this month.
Baxter Healthcare Corporation has 311 FDA actions in our database, including 288 recalls and 23 clearances.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Baxter Healthcare Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Baxter Healthcare Corporation have FDA actions?
Baxter Healthcare Corporation has 311 FDA actions in our database, including 288 recalls and 23 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "4c81b3a9-81ee-4bed-bfb3-1300b7ef3299" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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