Akron Pharma, Inc.: Drug Recall
Recall #D-0197-2025 · 12/12/2024
Class III: Low Risk
Recall Details
- Recall Number
- D-0197-2025
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Akron Pharma, Inc.
- Status
- Ongoing
- Date Initiated
- 12/12/2024
- Location
- Fairfield, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7198 bottles
Reason for Recall
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Product Description
Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8028-1.
Distribution Pattern
Nationwide in the US
Other Recalls by Akron Pharma, Inc.
- Class III: Low Risk 12/12/2024
- Class III: Low Risk 12/12/2024
- Class III: Low Risk 12/12/2024
- Class III: Low Risk 12/12/2024
- Class III: Low Risk 12/12/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.