Why it was recalled
Discoloration
Product description
Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Made in Ireland, NDC 36000-306-60.
Lot numbers, UPCs & expiration codes
Lot #: 24A27G66, Exp 12/31/2025
Where it was sold
U.S.A. 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-0596-2025
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Aug 20, 2025
- FDA report date
- Sep 3, 2025
- Quantity
- 13,000 containers
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Baxter Healthcare Corporation
Original FDA data
Every field from FDA enforcement report D-0596-2025, exactly as published.
Show all FDA fields
- City
- Deerfield
- State
- IL
- Status
- Ongoing
- Country
- United States
- Event ID
- 97453
- Address
- 1 Baxter Pkwy
- Code information
- Lot #: 24A27G66, Exp 12/31/2025
- Postal code
- 60015-4625
- Report date
- Sep 3, 2025
- Product type
- Drugs
- Recall number
- D-0596-2025
- Classification
- Class II
- Recalling firm
- Baxter Healthcare Corporation
- Product quantity
- 13,000 containers
- Reason for recall
- Discoloration
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Made in Ireland, NDC 36000-306-60.
- Distribution pattern
- U.S.A. Nationwide
- Recall initiation date
- Aug 20, 2025
- Initial firm notification
- Letter
- Center classification date
- Aug 22, 2025