Recall
FDAHealthDecember 12, 2024

Akron Pharma, Inc. — 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.

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
December 12, 2024

Nationwide in the US

What's affected?

Product
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.
Lot code
KDT0224002A

Additional details

Lot: KDT0224002A, Exp 09/30/2026

What should I do?

Recommended action

Class III recall. Voluntary: Firm initiated Quantity affected: 768 bottles.

View original FDA notice →

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