Ultra Seal Corporation recalls Sinus Relief Headache/Nasal tablets due to cGMP deviations. Affected lots include AK9436 (expiring 01/2022).
cGMP deviations
Ultra Seal Corporation is recalling Sinus Relief Headache/Nasal tablets that were manufactured for Select Corporation. The recall is due to cGMP deviations, which means the product may not meet quality standards.
cGMP deviations refer to failures in the manufacturing process that could affect product quality. This means the tablets might not be safe or effective as intended.
People who purchased Sinus Relief Headache/Nasal tablets with lot number AK9436 (expiring 01/2022) are affected. Those using the product for nasal congestion or headaches may be at risk.
Check the lot number on the packaging, which should be AK9436 for this recall. The product was manufactured for Select Corporation and expires on January 2022.
Look for the lot number AK9436 on the packaging to confirm if your product is affected.
Ultra Seal Corporation is recalling Sinus Relief Headache/Nasal tablets with lot number AK9436 due to cGMP deviations.
Check the lot number on the packaging; affected products have lot number AK9436 and expire on January 2022.
The recall record does not specify a remedy, so contact Ultra Seal Corporation directly for guidance.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0519-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0519-2022 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.
