Ultra Seal Corporation recalls Backache & Muscle Relief tablets due to cGMP deviations. Affected lots expired by 2022. Consumers should check product details and contact for remedy.
cGMP deviations
Ultra Seal Corporation is recalling Backache & Muscle Relief tablets because of manufacturing quality issues. This recall affects specific batches that expired by August 2022. The issue could lead to unsafe product quality, but no injuries have been reported.
The product was made with cGMP (current Good Manufacturing Practice) deviations, which means the quality control process failed. This could result in unsafe levels of ingredients or impurities in the tablets. However, the specific risk to consumers is not clearly described in the recall notice.
People who bought the Backache & Muscle Relief tablets from First Aid Direct in Mason, Ohio between 2021 and 2022 are affected. Those using the product without checking the batch number are at risk.
Check the product label for the batch number (e.g., K9770, AK9770) and expiration date (by August 2022 or December 2022). The product was manufactured for First Aid Direct in Mason, Ohio.
Look for the batch number (e.g., K9770) and expiration date on the label.
Ultra Seal Corporation is recalling Backache & Muscle Relief tablets due to cGMP deviations in manufacturing.
Batches with batch numbers K9770, AK9770 (exp. 08/2022), AK9958 (exp. 12/2022), AK9717 (exp. 07/2022), AK9522 and AK9641 (exp. 03/2022), and AK9817 (exp. 09/2022).
Check the product label for the batch number and expiration date. If affected, contact Ultra Seal Corporation for instructions.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0482-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0482-2022 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.
