ULTRAtab recalls bulk peppermint antacid tablets due to CGMP deviations. Affected lots from 19C042 to 19F083 may pose quality risks.
CGMP Deviations
ULTRAtab is recalling bulk peppermint antacid tablets that were produced with CGMP deviations. This means the tablets may not meet quality standards, though serious harm is not expected.
CGMP deviations refer to failures in the manufacturing process that could affect product quality. This means the tablets might not meet the required standards for safety and effectiveness, but serious injury is not a direct risk.
People who bought the bulk peppermint antacid tablets with NDC 62959-303-00 from ULTRAtab Laboratories in Highland, NY. Those most at risk are users of the product in bulk form.
Check for the product code M303 or M303A with bulk lots 19C042, 19C043, 19F083, or 19E105. The product is a bulk container of peppermint antacid tablets with NDC 62959-303-00.
Verify the product code and lot numbers listed in the recall notice to confirm if your tablets are affected.
The recall is due to CGMP deviations, which may affect product quality but do not indicate a risk of serious injury.
Look for the product code M303 or M303A with bulk lots 19C042, 19C043, 19F083, or 19E105 on the container.
The recall does not require immediate action; check the product details to confirm if it's affected.
We’ve drafted a message you can send ULTRAtab to request your refund or repair — edit it as you like.
Subject: Recall D-0539-2022 — ULTRAtab ULTRAtab Hello, I own a ULTRAtab that is covered by recall D-0539-2022 from ULTRAtab. 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.
