Akron Pharma, Inc. 2025-01-22 Health moderate FDA
Health · FDA · Recall #FDA-D-0199-2025
Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for:… Recall
Issued January 22, 2025 · Akron Pharma, Inc.
In January 2025, Akron Pharma, Inc. recalled the Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for:…, a moderate health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
What you should do
- 1 Stop using Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for:… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Akron Pharma, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Akron Pharma, Inc.
- Category
- Health
- Recall date
- January 22, 2025
- Units affected
- Not reported
- Sold at
- Nationwide in the US
- Recall number
- FDA-D-0199-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Akron Pharma, Inc. has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.