Home / drug / D-0196-2025 Class III Reported 2025-01-22
Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02 Recalled by Akron Pharma, Inc.
Reason for Recall Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
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Recall Number D-0196-2025
Classification Class III
Status Ongoing
Category drug
Initiated 2024-12-12
Reported 2025-01-22
Distribution Nationwide in the US
Code Info Lot #s: KDT0224001B, Exp 08/31/2026; KDT0224002B, Exp 09/30/2026. Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer .