Why it was recalled
Presence of Particulate Matter
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 numbers, UPCs & expiration codes
Lot # LD175708, Exp Date: 14-Feb-2027.
Where it was sold
US Nationwide.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0787-2026
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- Jul 24, 2026
- FDA report date
- Aug 19, 2026
- Quantity
- 19,032 bags
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Baxter Healthcare Corporation
Original FDA data
Every field from FDA enforcement report D-0787-2026, exactly as published.
Show all FDA fields
- City
- Deerfield
- State
- IL
- Status
- Ongoing
- Country
- United States
- Event ID
- 99463
- Address
- 1 Baxter Pkwy
- Code information
- Lot # LD175708, Exp Date: 14-Feb-2027.
- Postal code
- 60015-4625
- Report date
- Aug 19, 2026
- Product type
- Drugs
- Recall number
- D-0787-2026
- Classification
- Class I
- Recalling firm
- Baxter Healthcare Corporation
- Product quantity
- 19,032 bags
- Reason for recall
- Presence of Particulate Matter
- Voluntary / mandated
- Voluntary: Firm initiated
- 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.
- Distribution pattern
- US Nationwide.
- Recall initiation date
- Jul 24, 2026
- Initial firm notification
- Letter
- Center classification date
- Aug 21, 2026