Akron Pharma recalls extra-strength acetaminophen tablets with missing "AP 325" imprint. These tablets may be misidentified as different products, leading to incorrect dosing. Consumers should check for the imprint and contact the manufacturer for details.
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Akron Pharma is recalling extra-strength acetaminophen tablets that lack the "AP 325" imprint. This missing imprint could lead to misidentification and incorrect dosing, which might cause harm if taken without proper understanding of the product.
The tablets lack the "AP 325" imprint, which is a specific identifier. Without this imprint, the tablets may be confused with other products, potentially leading to incorrect dosing. This could cause harm if the wrong medication is taken.
Anyone who owns or uses the recalled acetaminophen tablets. People taking the medication for pain or fever may be at risk if the tablets are misidentified.
Check for the "AP 325" imprint on the tablet. The recalled products are extra-strength acetaminophen tablets in 100-count or 1000-count bottles with specific NDC numbers.
Look for the "AP 325" imprint on the tablet. If missing, the product is recalled.
The tablets lack the "AP 325" imprint, which could lead to misidentification and incorrect dosing.
Check for the "AP 325" imprint. If missing, stop using the product and contact Akron Pharma for details.
The recalled product may be misidentified, leading to incorrect dosing. However, the hazard is low risk as the tablets are not defective and the issue is about identification.
We’ve drafted a message you can send Akron Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-1353-2022 — Akron Pharma Akron Pharma Hello, I own a Akron Pharma that is covered by recall D-1353-2022 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.
