Diphenhydramine HCl 25 mg recall: Labeling Error
Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117…
Why was Diphenhydramine HCl 25 mg recalled?
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot: KDC0124001A Exp 09/30/2026.
- Product
- Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117…
- Recalling firm
- Akron Pharma, Inc.
- Quantity
- 7198 bottles
- Distribution
- Nationwide in the US
- Recall date
- January 22, 2025
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (drug)