Akron Pharma recalls 50mg diphenhydramine capsules with incorrect labeling. This could lead to confusion about the product's identity. Consumers should check the label and contact the company for details.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Akron Pharma is recalling 50mg diphenhydramine capsules that have incorrect labeling. This means consumers might be using the wrong product, which could lead to confusion about the medication's identity.
The capsules have incorrect labeling, which could cause confusion about the product's identity. This might lead to someone using the wrong medication instead of the intended diphenhydramine. However, the risk is low since the issue is only with labeling and not the product's safety.
People who own or use the recalled diphenhydramine capsules with the specific lot number KDC0224001B. Those most at risk are individuals who may have taken the wrong medication due to labeling confusion.
Check for the label that says 'Diphenhydramine HCl 50 mg, 1000 capsules per bottle' and the lot number KDC0224001B. The product was manufactured for Akron Pharma, Inc. in Fairfield, NJ.
Look for the lot number KDC0224001B on the product label to confirm if it is recalled.
The product is safe to use if it has the correct labeling. However, the recalled capsules have incorrect labeling, which could cause confusion about the product's identity.
Check the label for the lot number KDC0224001B. If you have this specific lot, contact Akron Pharma for further instructions.
Look for the label that says 'Diphenhydramine HCl 50 mg, 1000 capsules per bottle' and the lot number KDC0224001B on the product.
We’ve drafted a message you can send Akron Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0199-2025 — Akron Pharma Akron Pharma Hello, I own a Akron Pharma that is covered by recall D-0199-2025 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.
