Akron Pharma recalls 325mg acetaminophen tablets with incorrect labeling. Wrong ID on tablets may cause confusion with other products. Affected lots: KDT0124004-006, expiring 08/31/2026.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Akron Pharma is recalling 325mg acetaminophen tablets that have incorrect labeling. This could lead to confusion with other products, potentially causing the wrong medication to be taken.
The tablets have incorrect labeling that may cause confusion with other products. This could lead to taking the wrong medication if someone mistakenly uses these tablets instead of the intended product.
People who purchased the recalled acetaminophen tablets from pharmacies or online retailers. Those who have the specific lot numbers (KDT0124004-006) and expiration date (08/31/2026) are most at risk.
Check for the lot numbers KDT0124004, KDT0124005, or KDT0124006 on the packaging. The product expires on 08/31/2026. The tablets are 325mg per tablet, 100 tablets per bottle.
Verify the lot number on the packaging to see if it matches KDT0124004, KDT0124005, or KDT0124006.
The product has incorrect labeling that may cause confusion with other products, potentially leading to the wrong medication being taken.
Check the lot number on the packaging. If it matches KDT0124004, KDT0124005, or KDT0124006, contact Akron Pharma for guidance.
The recall is for labeling issues, not a safety hazard. There is no risk of serious injury from this 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-0195-2025 — Akron Pharma Akron Pharma Hello, I own a Akron Pharma that is covered by recall D-0195-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.