Akron Pharma, Inc. recalls Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (
Recalled August 24, 2022 · FDA recall D-1353-2022 · Akron Pharma
Hazard
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet. · FDA Class III
Units
30,325 bottles
Sold at
Product was distributed to 6 distributors/wholesalers who may have further distributed the product.
Description
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Product
Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC 71399-8022-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ
Manufacturer(s)
Akron Pharma, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →