Recall
FDAHealthDecember 12, 2024

Akron Pharma, Inc. — Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.

⚠️ 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, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.
Lot code
KDT0124004

Additional details

Lot #s: KDT0124004, KDT0124005, KDT0124006, Exp 08/31/2026

What should I do?

Recommended action

Class III recall. Voluntary: Firm initiated Quantity affected: 14825 bottles.

View original FDA notice →

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