FDAFDA · Food and drugs·Recall number D-0196-2025
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
Published January 22, 2025 · Recall initiated: December 12, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Akron Pharma, Inc.
- Distributor
- Nationwide in the US
- Lot
- Lot #s: KDT0224001B, Exp 08/31/2026; KDT0224002B, Exp 09/30/2026.
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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