Akron Pharma recalls 1000-tablet acetaminophen bottles with incorrect labeling. Wrong ID on tablets may cause confusion with other products. Consumers should check NDC 71399-8022-02 and lot numbers.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Akron Pharma is recalling 1000-tablet acetaminophen extra strength 500mg bottles due to incorrect labeling. This could lead to confusion with other products, but the recall does not indicate a safety risk to health.
The tablets have an incorrect ID imprint, which could lead to confusion with other products. This labeling error does not pose a direct health risk but may cause users to take the wrong medication.
People who own or use the recalled acetaminophen tablets with NDC 71399-8022-02 and lot numbers KDT0224001B (exp 08/31/2026) or KDT0224002B (exp 09/30/2026) are affected. Those most at risk are individuals who may confuse these tablets with other products due to incorrect labeling.
Check for NDC code 71399-8022-02 and lot numbers KDT0224001B (expiring 08/31/2026) or KDT0224002B (expiring 09/30/2026) on the bottle. The product is manufactured by Akron Pharma Inc. in Fairfield, NJ.
Look for NDC 71399-8022-02 and lot numbers KDT0224001B or KDT0224002B on the bottle.
The recall is due to incorrect labeling, not a safety risk. The product is safe to use but may be confused with other products.
The recall does not specify a remedy, so no action is required beyond checking the label for the NDC and lot numbers.
Check for NDC 71399-8022-02 and lot numbers KDT0224001B (exp 08/31/2026) or KDT0224002B (exp 09/30/2026) on the bottle.
We’ve drafted a message you can send Akron Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0196-2025 — Akron Pharma Akron Pharma Hello, I own a Akron Pharma that is covered by recall D-0196-2025 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.
