PlainRecalls
FDA Drug Moderate Class II Ongoing

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.

Reported: September 3, 2025 Initiated: August 20, 2025 #D-0596-2025

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

Details

Units Affected
13,000 containers
Distribution
U.S.A. Nationwide
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
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.. Recalled by Baxter Healthcare Corporation. Units affected: 13,000 containers.
Why was this product recalled?
Discoloration
Which agency issued this recall?
This recall was issued by the FDA Drug on September 3, 2025. Severity: Moderate. Recall number: D-0596-2025.