Baxter Healthcare Corporation recalls Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corp…

Recall date

August 20, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0596-2025

FDA classification

Class II

Brand / firm

Baxter Healthcare Corporation

Sold / distributed

U.S.A. Nationwide

Why it was recalled

Discoloration

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What 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.