PlainRecalls
FDA Drug Low Class III Terminated

Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC 71399-8024-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ

Reported: August 24, 2022 Initiated: August 4, 2022 #D-1352-2022

Product Description

Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC 71399-8024-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ

Reason for Recall

Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.

Details

Recalling Firm
Akron Pharma, Inc.
Units Affected
301,382 bottles
Distribution
Product was distributed to 6 distributors/wholesalers who may have further distributed the product.
Location
Fairfield, NJ

Frequently Asked Questions

What product was recalled?
Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC 71399-8024-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ. Recalled by Akron Pharma, Inc.. Units affected: 301,382 bottles.
Why was this product recalled?
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 24, 2022. Severity: Low. Recall number: D-1352-2022.