Sato Pharmaceutical recalls 75-count INON ACE antacid tablets with failed disintegration specifications. This may affect safety and effectiveness of the medication.
Failed Disintegration Specifications: above the time expected.
Sato Pharmaceutical is recalling 75-count INON ACE antacid tablets that failed disintegration tests. This could mean the tablets don't dissolve properly in the stomach, potentially reducing their effectiveness as an antacid.
The tablets failed disintegration specifications, meaning they don't dissolve in the stomach as intended. This could reduce their effectiveness as an antacid. However, the risk of serious harm is low since the tablets are designed to be taken with water and the failure is not expected to cause immediate injury.
People who own or use the recalled 75-count INON ACE antacid tablets. Those with digestive issues may be at slightly higher risk if the tablets don't dissolve properly.
Check for the 75-count bottle labeled 'INON ACE Antacid' with NDC 49873-402-01. The lot number PWXT and expiration date 1/31/2027 are also associated with this recall.
Verify the product label for the 75-count bottle with NDC 49873-402-01 and lot number PWXT.
The recall is due to failed disintegration specifications, which may reduce effectiveness but does not pose a serious injury risk.
The recall record does not specify a remedy, so no action is required beyond checking if you have the recalled product.
The product was manufactured with lot number PWXT and expires January 31, 2027.
We’ve drafted a message you can send Sato Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0298-2026 — Sato Pharmaceutical Sato Pharmaceutical Hello, I own a Sato Pharmaceutical that is covered by recall D-0298-2026 from Sato Pharmaceutical. 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.
