Akron Pharma recalls

4 official recalls and safety alerts involving Akron Pharma since 2022-08, from FDA · Drug. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Akron Pharma or the relevant agency.

1. 2025-01-22
2. US
   Drugs & medicalClass III

   Akron Pharma, Inc. recalls Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC…

   Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

   FDA · DrugAkron Pharma, Inc.Nationwide in the USOfficial notice →
3. 2024-10-30
4. US
   Drugs & medicalClass II

   Akron Pharma, Inc. recalls OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Pharma, Manufactured…

   CGMP Deviations

   FDA · DrugAkron Pharma, Inc.Nationwide in the USOfficial notice →
5. 2023-03-15
6. US
   Drugs & medicalClass III

   Akron Pharma, Inc. recalls DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1

   Labeling: Incorrect or Missing Lot and/or Exp Date

   FDA · DrugAkron Pharma, Inc.Nationwide within the United StatesOfficial notice →
7. 2022-08-24
8. US
   Drugs & medicalClass III

   Akron Pharma, Inc. recalls Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC…

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

   FDA · DrugAkron Pharma, Inc.Product was distributed to 6 distributors/wholesalers who may have further…Official notice →