INON ACE Antacid tablets (magnesium aluminosilicate, magnesium hydroxide and simethicone), 75-count bottle, NDC 49873-402-01, Lot PWXT, Exp 1/31/2027, manufactured by Sato Pharmaceutical Co., Ltd., are being recalled. The recall was issued because the tablets failed disintegration specifications (above the time expected) and affects 3,640 bottles sold in California and Hawaii.
What's being recalled
INON ACE Antacid tablets (magnesium aluminosilicate, magnesium hydroxide and simethicone), 75-count bottle, Manufactured by: Sato Pharmaceutical Co., Ltd., NDC 49873-402-01
Recalling firm: Sato Pharmaceutical Co., Ltd, Tokyo, N/A, Japan.
How to identify it
Lot#: PWXT, Exp 1/31/2027
The hazard
Failed Disintegration Specifications: above the time expected.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
CA and HI
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)