Ultra Seal Corporation recalls headache and congestion relief tablets due to manufacturing quality issues. Affected products include specific lots from 2022 with NDC 42961-0206-02. Consumers should check labels for lot numbers and expiration dates.
cGMP deviations
Ultra Seal Corporation is recalling headache and congestion relief tablets that were made with manufacturing quality issues. This recall affects specific lots produced between 2022 with certain expiration dates and lot numbers. The issue could lead to unsafe product quality, but the recall does not specify immediate health risks.
The product was made with manufacturing quality issues (cGMP deviations) that could affect safety. However, the recall does not specify how these issues could cause harm or what the exact risk is.
People who purchased the affected headache and congestion relief tablets from stores or online. Those who used the product before the expiration date are most at risk.
Check the product label for the lot number and expiration date. The affected products have specific lot numbers like AK9445, K9445, and expiration dates from January 2022 through September 2022.
Look for the lot number and expiration date on the packaging to determine if the product is affected.
The products were made with manufacturing quality issues (cGMP deviations), but the recall does not specify how this affects safety.
Check the product label for lot numbers like AK9445, K9445, or K9810 and expiration dates from January 2022 through September 2022.
The recall does not specify a remedy, so you should check the product label and contact Ultra Seal Corporation for further 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-0484-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0484-2022 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.
