Class IIIReported 2025-01-22
Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.
Recalled by Akron Pharma, Inc.
Reason for Recall
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
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Recall NumberD-0195-2025ClassificationClass IIIStatusOngoingCategorydrugInitiated2024-12-12Reported2025-01-22DistributionNationwide in the USCode InfoLot #s: KDT0124004, KDT0124005, KDT0124006, Exp 08/31/2026Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.