Ultra Seal Corporation recalls DILOTAB II cold relief tablets due to cigarette manufacturing deviations. Affected lots expire by April 2022 and June 2022. Stop using immediately.
cGMP deviations
Ultra Seal Corporation is recalling DILOTAB II cold relief tablets that contain acetaminophen and phenylephrine. The recall is due to cigarette manufacturing deviations, which may pose a risk of serious injury.
The recall is for cigarette manufacturing deviations, which means the tablets may not be produced safely. This could lead to serious injury if the tablets are taken incorrectly.
People who own or use DILOTAB II cold relief tablets with the specific lot numbers listed in the recall notice are affected. Those who have the tablets with expiration dates up to April 2022 or June 2022 are at risk.
Check the product label for the lot numbers AK9548, AK9647, or AK9598. The expiration dates for these lots are April 2022, June 2022, or May 2022.
Discard the recalled DILOTAB II cold relief tablets if you have them.
The recall is due to cigarette manufacturing deviations, which may pose a risk of serious injury.
Check the product label for lot numbers AK9548, AK9647, or AK9598 with expiration dates up to April 2022 or June 2022.
The recall does not specify a return process, so you should discard the tablets immediately.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0490-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0490-2022 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.
