WhichRecall
Class IIIReported 2025-01-22

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.

Recalled by Akron Pharma, Inc.

Reason for Recall

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

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Recall Number
D-0197-2025
Classification
Class III
Status
Ongoing
Category
drug
Initiated
2024-12-12
Reported
2025-01-22
Distribution
Nationwide in the US
Code Info
Lot: KDC0124001A Exp 09/30/2026.
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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