Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Over-the-Counter

INON ACE Antacid Tablets Recalled for Failed Disintegration

Agency Publication Date: January 27, 2026
Share:
Sign in to monitor this recall

Summary

Sato Pharmaceutical Co., Ltd. is recalling 3,640 bottles of INON ACE Antacid tablets (magnesium aluminosilicate, magnesium hydroxide, and simethicone) because the tablets failed to break down (disintegrate) within the expected timeframe. This issue affects 75-count bottles from lot PWXT that were distributed in California and Hawaii. Because the tablets do not dissolve as intended, they may not provide the expected relief for digestive symptoms.

Risk

The tablets do not break down properly in the digestive tract, which means the active ingredients may not be released effectively, potentially resulting in a lack of treatment for the consumer's symptoms.

What You Should Do

  1. Check your bottle for INON ACE Antacid tablets, 75-count size, with NDC 49873-402-01 and Lot Number PWXT with an expiration date of 1/31/2027.
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: INON ACE Antacid tablets (75-count bottle)
Variants: Magnesium aluminosilicate, Magnesium hydroxide, Simethicone
Lot Numbers:
PWXT (Exp 1/31/2027)
NDC:
49873-402-01

Recall #: D-0298-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98216
Status: Active
Manufacturer: Sato Pharmaceutical Co., Ltd
Manufactured In: Japan
Units Affected: 3,640 bottles
Distributed To: California, Hawaii

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.