Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Akron Pharma, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1352-2022 — Akron Pharma, Inc. Akron Pharma, Inc. recalls Acetaminophen 325 mg tablets, packaged in a) 100-coun Hello, I own a Akron Pharma, Inc. recalls Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC that is covered by recall D-1352-2022 from Akron Pharma, Inc.. 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.
