US Drug Recall Register
Class II · Moderate risk Completed Initiated Mar 24, 2022 (4 years ago)

Acetaminophen Oral Solution, USP 650mg/ 20.3 mL cup, packaged in 10 cups per tray, 10…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Failure to properly investigate failed microbial testing.

What was recalled

Acetaminophen Oral Solution, USP 650mg/ 20.3 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC: 0904-6820-76.

Recalling firm
Plastikon Healthcare LLC
Origin
KS, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0869-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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