Ultra Seal Corporation recalls Back Pain-Off tablets due to manufacturing quality deviations. Affected lots expired by July 2022. Consumers should check product labels for specific lot numbers and expiration dates.
cGMP deviations
Ultra Seal Corporation is recalling Back Pain-Off pain relief tablets that were manufactured with quality control issues. This recall affects specific batches that expired by July 2022. The issue does not involve immediate safety risks but requires consumers to check their product labels.
The tablets were produced with cGMP (current Good Manufacturing Practice) deviations, meaning the manufacturing process did not meet quality standards. This could lead to inconsistent medication content or potential safety issues, though the recall does not indicate immediate harm to consumers.
People who own or use Back Pain-Off tablets from Ultra Seal Corporation, particularly those with specific lot numbers and expiration dates listed in the recall. Those who have the affected batches are most at risk.
Check the product label for the lot number and expiration date. Affected lots include AK9810 (exp. 07/2022), AK9946 (exp. 12/2022), and others as listed in the recall notice.
Look for the lot number and expiration date on the tablet packaging.
The recall is due to manufacturing quality deviations, not immediate safety risks. The tablets are not considered dangerous but should be checked for the specific lot numbers.
Check the product label for lot numbers AK9810 (exp. 07/2022), AK9946 (exp. 12/2022), or other specific lots listed in the recall notice.
The recall does not require stopping use immediately. Consumers should check the product label for the specific lot numbers and expiration dates to determine if their tablets are affected.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0476-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0476-2022 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.
