Ultra Seal recalls Extra Strength acetaminophen pain relievers with cGMP deviations. Affected lots may cause safety issues.
cGMP deviations
Ultra Seal is recalling Extra Strength pain relievers (acetaminophen 50:00 mg) due to manufacturing quality issues. This could lead to safety risks if the product is used.
The product was made with cGMP (current Good Manufacturing Practices) deviations, which means the manufacturing process did not meet quality standards. This could lead to safety issues if the product is used.
People who bought the Extra Strength pain relievers with lot number AK9602, expiring May 2022, are affected. Those using the product regularly are most at risk.
Check for the lot number AK9602 on the packaging, which expires May 2022. The product is an Extra Strength acetaminophen pain reliever in 2-tablet packets.
Look for the lot number AK9602 and expiration date of May 2022 on the packaging.
The product was made with cGMP deviations, which means the manufacturing process did not meet quality standards.
The official recall notice does not specify a remedy or action for affected products.
The recall record does not describe a specific hazard that could cause serious injury.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0469-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0469-2022 from Ultra Seal. 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.
