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Recall Observatory FDA recall evidence

Drug product

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

D-0196-2025

December 12, 2024

Class III

Product summary

Firm
Akron Pharma, Inc.
Event
Event 95944
Status
Ongoing
Classification
Class III
Quantity
1232 bottles
Official record key
drug-enforcement:D-0196-2025

Official wording

Reason: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Code information: Lot #s: KDT0224001B, Exp 08/31/2026; KDT0224002B, Exp 09/30/2026.

Distribution pattern: Nationwide in the US

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.