FDAFDA · Food and drugs·Recall number D-0199-2025
Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US 46, Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8026-02.
Published January 22, 2025 · Recall initiated: December 12, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Akron Pharma, Inc.
- Distributor
- Nationwide in the US
- Lot
- Lot: KDC0224001B Exp 09/30/2026
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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