Ultra Seal recalls COLD TERMINATOR cold relief tablets due to cGMP deviations. Affected lots manufactured in Carlsbad, CA with NDC 69103-2556. No remedy specified in official notice.
cGMP deviations
Ultra Seal is recalling COLD TERMINATOR cold relief tablets that were made with cGMP deviations. This means the product may not meet quality standards, but the recall does not specify a remedy or hazard that could cause injury.
cGMP deviations refer to failures in manufacturing quality control processes. This could mean the product does not meet safety or quality standards, but the recall does not specify how this leads to injury or harm.
People who bought COLD TERMINATOR cold relief tablets with NDC 69103-2556 from Tellus Medical Products in Carlsbad, CA. Those who used the product after the expiration date of 02/2022 are at higher risk.
Check for the product name 'COLD TERMINATOR' with acetaminophen 325 mg, guaifenesin 200mg, and phenylephrine HCl. Look for the lot number AK9587 and expiration date 02/2022 on the packaging.
Identify the product by checking the label for NDC 69103-2556 and lot number AK9587.
The recall mentions cGMP deviations but does not specify any hazard that could cause injury.
The official notice does not specify a remedy or action for the product.
The product was manufactured with lot number AK9587 and expired on 02/2022.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0487-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0487-2022 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.