Akron Pharma, Inc. recalls Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W…
- Recall date
- December 12, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0197-2025
- FDA classification
- Class III
- Brand / firm
- Akron Pharma, Inc.
- Sold / distributed
- Nationwide in the US
Why it was recalled
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
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.
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