Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Acetaminophen Recalled by Akron Pharma, Inc. Due to Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Akron Pharma, Inc. directly.
Affected Products
Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.
Quantity: 14825 bottles
Why Was This Recalled?
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Akron Pharma, Inc.
Akron Pharma, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report