US Drug Recall Register
Class II · Moderate risk Ongoing Initiated May 20, 2024 (2 years ago)

Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR…

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

Why it was recalled

Discoloration: Brownish tablets

What was recalled

Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR PHARMACEUTICALS, 17177 N Laurel Park Drive, Suite 233, Livonia, MI USA 48152, NDC 0904-6730-60, UPC Number 309046730606

Recalling firm
Contract Pharmacal Corporation
NDC code
0904-6730-60
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0566-2024

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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