Akron Pharma, Inc. recalls Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US
Recalled January 22, 2025 · FDA recall D-0196-2025 · Akron Pharma
Hazard
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. · FDA Class III
Units
1232 bottles
Sold at
Nationwide in the US
Description
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Product
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
Manufacturer(s)
Akron Pharma, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →