Ultra Seal Corporation recalls CHLORESIN 2-tablet packets manufactured with cGMP deviations. Affected lots include AK9492 (expiring 02/2022).
cGMP deviations
Ultra Seal Corporation is recalling CHLORESIN 2-tablet packets that were manufactured with cGMP deviations. This means the product may not meet quality standards, though the specific risk isn't detailed in the recall.
The recall mentions cGMP deviations, which are quality control issues in drug manufacturing. However, the specific hazard mechanism isn't described in the record, so the risk level cannot be determined.
People who purchased CHLORESIN 2-tablet packets from Ultra Seal Corporation. Those with the specific lot number AK9492 (expiring 02/2022) are most at risk.
Check for CHLORESIN 2-tablet packets with lot number AK9492 that expire on 02/2022. The product was manufactured by Ultra Seal Corporation for Afassco Inc. in Minden, NV.
Look for the lot number AK9492 on the packaging, which expires on 02/2022.
The recall states there were cGMP deviations, but does not specify if the product is unsafe. The official notice does not detail the specific risk.
The recall does not provide a remedy, so there is no action required beyond checking if you have the affected lot.
Check the lot number on the packaging; affected products have lot number AK9492 that expires on 02/2022.
We’ve drafted a message you can send Ultra Seal Corporation to request your refund or repair — edit it as you like.
Subject: Recall D-0468-2022 — Ultra Seal Corporation Ultra Seal Corporation Hello, I own a Ultra Seal Corporation that is covered by recall D-0468-2022 from Ultra Seal Corporation. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.