Ultra Seal Corporation recalls Nutralox Mint Antacid chewable tablets due to cGMP deviations. Affected lots from April 2022 expire May 2022. No specific remedy stated in official notice.
cGMP deviations
Ultra Seal Corporation is recalling Nutralox Mint Antacid chewable tablets that were manufactured for HARTHealth in Seattle, WA. The recall is due to cGMP deviations, which are quality control issues that could affect safety. This recall does not include all products but specific lots with expiration dates in April and May 2022.
cGMP deviations refer to quality control failures in manufacturing that could lead to unsafe products. While the exact risk isn't specified, such deviations might affect the product's safety or effectiveness.
People who purchased Nutralox Mint Antacid chewable tablets from HARTHealth in Seattle, WA between the specified dates. Those who have the affected lots (AK9566 or AK9612) are most at risk.
Check for Nutralox Mint Antacid chewable tablets in 2-count packets manufactured for HARTHealth in Seattle, WA. Look for lot numbers AK9566 (expires April 2022) or AK9612 (expires May 2022).
Identify if you have Nutralox Mint Antacid chewable tablets with lot numbers AK9566 or AK9612 from HARTHealth in Seattle, WA.
The recall is due to cGMP deviations, which are quality control issues that could affect safety.
The official notice does not specify a remedy, so you should check the product details and contact the manufacturer if you have the affected lots.
No, only specific lots with lot numbers AK9566 (expires April 2022) and AK9612 (expires May 2022) 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-0508-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0508-2022 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.
