FDAFDA · Food and drugs·Recall number D-0194-2025
Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8024-01 .
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 #: KDT0124001, Exp 08/31/2026
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.