inon acedrugHigh PriorityActive

INON ACE Antacid tablets (magnesium aluminosilicate, magnesium hydroxide and simethicone), 75-count bottle, Manufactured by: Sato Pharmaceutical Co., Ltd., NDC 49873-402-01

inon ace INON ACE Antacid tablets (magnesium aluminosilicate, magnesium hydroxide and simethicone), 75-count bottle, Manufactured by: Sato Pharmaceutical Co., Ltd., NDC 49873-402-01 recalled by FDA. Failed Disintegration Specifications: above the time expected.

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: December 19, 2025
Last reviewed by RecallRadar: March 4, 2026

What You Should Do

1## INON ACE Antacid tablets (magnesium aluminosilicate, magnesium hydroxide and simethicone), 75-count bottle, Manufactured by: Sato Pharmaceutical Co., Ltd., NDC 49873-402-01 Agency: FDA | Category: drug Reason: Failed Disintegration Specifications: above the time expected. What to do:
2Stop using the product if your lot/model matches.
3Check the FDA notice for specifics.
4Follow remedy instructions.

Open Official Recall Notice Get Alerts for inon ace Devices

What's Being Recalled

Quoted source excerpt from the official notice.

Failed Disintegration Specifications: above the time expected.

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Lot#: PWXT, Exp 1/31/2027

#	Model
1	Lot#: PWXT, Exp 1/31/2027

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my inon ace device affected?

Check the affected models section on this page. The official notice currently lists Lot#: PWXT, Exp 1/31/2027.

What is the remedy for this recall?

## INON ACE Antacid tablets (magnesium aluminosilicate, magnesium hydroxide and simethicone), 75-count bottle, Manufactured by: Sato Pharmaceutical Co., Ltd., NDC 49873-402-01 Agency: FDA | Category: drug Reason: Failed Disintegration Specifications: above the time expected. What to do: 1. Stop using the product if your lot/model matches. 2. Check the FDA notice for specifics. 3. Follow remedy instructions.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Keep browsing with these internal hubs: inon ace recall hub and Food & Drug recall hub.