Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Acetaminophen Extra Strength 500 mg 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 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
Quantity: 1232 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