FDA Drugs recall ·
Acetaminophen Injection 1000 mg/100 mL (10 mg/mL)… recall
- Recall number
- D-0596-2025
- Date
- (initiated August 20, 2025)
- Company / brand
- Baxter Healthcare Corporation
1 Baxter Pkwy, Deerfield, IL, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 13,000 containers
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
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.
Why was it recalled?
Discoloration
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot #: 24A27G66, Exp 12/31/2025
Distribution
U.S.A. Nationwide
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0596-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.