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
Buy Me a Coffee

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.

Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

Sun Pharmaceutical Industries, Inc.: Riomet (metformin hydrochloride) Oral Solution Recalled for Labeling Errors

Agency Publication Date: May 16, 2018
Share:
Sign in to monitor this recall

Summary

Sun Pharmaceutical Industries, Inc. is voluntarily recalling approximately 19,758 bottles of Riomet (metformin hydrochloride oral solution), 500 mg/5 mL, sold in 473 mL (16 fl. oz.) plastic bottles. The recall was initiated because of labeling discrepancies found in the patient literature included with the medication. These errors could lead to patients receiving incorrect information about how to use the drug or its safety profile. Riomet is a prescription medication used to treat type 2 diabetes.

Risk

Inaccurate information in patient literature may result in patients misunderstanding dosing instructions or safety warnings, potentially affecting the management of their blood sugar levels or overall health.

What You Should Do

  1. Check your prescription bottles to see if you have Riomet (metformin hydrochloride oral solution), 500 mg/5 mL in 473 mL plastic bottles with NDC 10631-206-02.
  2. Verify if your bottle matches one of the following lot numbers and expiration dates: E170210A (Exp 06/09/2019), F170214A (Exp 07/05/2019), F170223A (Exp 07/06/2019), F170224A (Exp 07/10/2019), F170231A (Exp 07/12/2019), or F170232A (Exp 07/13/2019).
  3. If you have an affected product, contact your healthcare provider or pharmacist immediately to discuss the labeling discrepancies and ensure you have the correct usage instructions.
  4. Return any unused portions of the affected medication to the pharmacy where you purchased it for a refund.
  5. Contact Sun Pharmaceutical Industries, Inc. at their distributor address in Cranbury, New Jersey, or visit the FDA website at www.fda.gov/safety/recalls for further information.
  6. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Riomet (metformin hydrochloride oral solution), 500 mg/5 mL (473 mL bottle)
Model:
NDC 10631-206-02
Lot Numbers:
E170210A (Exp 06/09/2019)
F170214A (Exp 07/05/2019)
F170223A (Exp 07/06/2019)
F170224A (Exp 07/10/2019)
F170231A (Exp 07/12/2019)
F170232A (Exp 07/13/2019)
Date Ranges: Exp 06/09/2019, 07/05/2019, Exp 07/06/2019, Exp 07/10/2019, Exp 07/12/2019, Exp 07/13/2019

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79979
Status: Resolved
Manufacturer: Sun Pharmaceutical Industries, Inc.
Manufactured In: United States
Units Affected: 19,758 473 mL bottles
Distributed To: Nationwide

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.