Home / drug / D-0193-2025 Class III Reported 2025-01-22
Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01. 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-0193-2025
Classification Class III
Status Ongoing
Category drug
Initiated 2024-12-12
Reported 2025-01-22
Distribution Nationwide in the US
Code Info Lot: KDT0224002A, Exp 09/30/2026 Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer .