D-0596-2025 Class II Ongoing
FDA drug recall D-0596-2025 was initiated by Baxter Healthcare Corporation on Aug 20, 2025 and is designated Class II. Reason for recall: Discoloration The recall status is ongoing. Affected quantity: 13,000 containers.
Recall Details
- Product Type
- Drugs
- Report Date
- Sep 3, 2025
- Initiation Date
- Aug 20, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 13,000 containers
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.
Reason for Recall
Discoloration
Distribution Pattern
U.S.A. Nationwide
Code Information
Lot #: 24A27G66, Exp 12/31/2025