Ultra Seal Corporation recalls mint-flavored antacid tablets due to cGMP deviations. Affected lots from March 2022 expire in June 2022. Consumers should check product labels for NDC 67060-303-68 and lot numbers AK9523 or AK9670.
cGMP deviations
Ultra Seal Corporation is recalling mint-flavored antacid tablets that may have manufacturing quality issues. This recall affects specific lots produced in March 2022 with expiration dates through June 2022. Consumers should check their product labels for the NDC number and lot codes listed.
The recall is due to cGMP deviations, which are manufacturing quality issues that may affect the safety and effectiveness of the product. These deviations could potentially lead to improper medication levels or other quality concerns, though the exact risk is not specified in the recall notice.
People who own or use the mint-flavored antacid tablets with the NDC 67060-303-68 and lot numbers AK9523 or AK9676 (expiring March 2022 or June 2022) are affected. Those who have these specific products are most at risk.
Check the product label for the NDC number 67060-303-68 and lot numbers AK9523 or AK9670. The expiration dates for these lots are March 2022 and June 2022 respectively.
Look for the NDC number 67060-303-68 and lot numbers AK9523 or AK9670 on the packaging.
The recall is due to cGMP deviations, which are manufacturing quality issues that may affect the product's safety and effectiveness.
Check the product label for the NDC number 67060-303-68 and lot numbers AK9523 or AK9670. If you have these specific products, contact Ultra Seal Corporation for further instructions.
The recall notice states there are cGMP deviations, but does not specify the exact safety risks or whether the product is dangerous in normal use.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0496-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0496-2022 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.
