Akron Pharma recalls 25mg diphenhydramine capsules with incorrect labeling that could lead to confusion about the product's identity.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Akron Pharma is recalling 25mg diphenhydramine capsules due to incorrect labeling. This could cause confusion about which product is being used, potentially leading to incorrect medication intake.
The capsules have the wrong labeling, meaning they might be mistaken for another product. This could lead to confusion about which medication is being taken, potentially causing incorrect dosing.
People who own or use these capsules are affected. Those who have the product with the specific lot number KDC0124001A are most at risk.
Check for the lot number KDC0124001A on the packaging. The product is labeled as Diphenhydramine HCl 25 mg, 100 capsules per bottle.
Look for the lot number KDC0124001A on the packaging to confirm if it's the recalled product.
The recall is due to incorrect labeling, not a safety hazard. The product itself is safe but may be confused with another product.
Check for the lot number KDC0124001A on the packaging. The product is labeled as Diphenhydramine HCl 25 mg, 100 capsules per bottle.
The recall does not require immediate action. Check the label to confirm if it's the recalled product and contact Akron Pharma if unsure.
We’ve drafted a message you can send Akron Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0197-2025 — Akron Pharma Akron Pharma Hello, I own a Akron Pharma that is covered by recall D-0197-2025 from Akron Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.