ULTRAtab recalls Spearmint Antacid Tablets (Calcium Carbonate 42:0 mg) due to CGMP deviations. This may affect safety and quality of the product.
CGMP Deviations
ULTRAtab is recalling Spearmint Antacid Tablets (Calcium Carbonate 420 mg) because of manufacturing quality issues. This recall does not involve immediate health risks but ensures product safety and quality.
CGMP deviations refer to manufacturing quality issues that could affect product safety and quality. These deviations may not cause immediate harm but are corrected to ensure product integrity.
People who purchased the Spearmint Antacid Tablets from ULTRAtab Laboratories, Inc. in Highland, NY. Those with the specific NDC code 62959-311-00 and product code M311 are most affected.
Check for the product name 'Spearmint Antacid Tablet (Calcium Carbonate 420 mg)', NDC code 62959-311-00, and product code M311. The bulk lot number 19A069 is also associated with this recall.
Review the NDC code (62959-311-00) and product code (M311) to confirm if your tablets are affected.
The recall is due to CGMP deviations, which may affect product safety and quality but do not pose immediate health risks.
Check for the NDC code 62959-311-00 and product code M311 on the packaging, or look for the bulk lot number 19A069.
The recall does not specify a remedy, so contact ULTRAtab Laboratories, Inc. for further instructions.
We’ve drafted a message you can send ULTRAtab to request your refund or repair — edit it as you like.
Subject: Recall D-0542-2022 — ULTRAtab ULTRAtab Hello, I own a ULTRAtab that is covered by recall D-0542-2022 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.
