Ultra Seal Corporation recalls extra strength PAIN TERMINATOR pain relief tablets due to cGMP deviations. Affected lots manufactured in Palm Desert, CA. No specific remedy stated in recall notice.
cGMP deviations
Ultra Seal Corporation is recalling extra strength PAIN TERMINATOR pain relief tablets that contain aspirin, acetaminophen, caffeine, and salicylamide. The recall is due to cGMP deviations, which means the product was made under quality control issues that could affect safety.
cGMP deviations refer to failures in the manufacturing process that could lead to unsafe products. These deviations might result in the product not meeting safety standards, potentially causing harm to users. However, the specific risk is not clearly described in the recall notice.
People who purchased the PAIN TERMINATOR extra strength pain relief tablets with the lot number AK9451 from Tellus Medical Products in Palm Desert, CA. Those using the product for pain relief are most at risk due to potential quality control issues.
Check for the lot number AK9451 on the packaging. The product was manufactured by Tellus Medical Products in Palm Desert, CA and expires January 2022. The product contains aspirin, acetaminophen, caffeine, and salicylamide.
Look for the lot number AK9451 on the packaging to confirm if your product is affected.
The recall notice does not state any remedy or action steps for consumers.
The recall mentions cGMP deviations but does not specify the exact risk or potential harm.
Check for the lot number AK9451 on the packaging. The product was manufactured by Tellus Medical Products in Palm Desert, CA and expires January 2022.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0488-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0488-2022 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.
