US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 16, 2021 (5 years ago)

Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle…

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

Why it was recalled

cGMP deviations: Discolored acetaminophen

What was recalled

Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10

Recalling firm
Spirit Pharmaceuticals
NDC code
79903-052-10
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0729-2021

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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