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.

Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

Acetazolamide Tablets Recalled for Discoloration

Agency Publication Date: September 30, 2024
Share:
Sign in to monitor this recall

Summary

Rubicon Research Private Limited has recalled 3,984 bottles of Acetazolamide (125 mg) tablets because of reports of tablet discoloration. This prescription medication is distributed by Advagen Pharma Limited in 100-count bottles. Consumers using this medication should speak with their doctor or pharmacist regarding their treatment and how to handle the affected product.

Risk

The recall was initiated because the tablets may show discoloration, which is a defect in the product's appearance and quality. While this is a low-risk recall, using discolored medication may lead to patient concern or potential changes in the drug's effectiveness.

What You Should Do

  1. This recall affects 100-count bottles of Acetazolamide Tablets, USP, 125 mg (NDC 72888-047-01) with lot number 30575HF1 and an expiration date of November 2026.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Rubicon Research Private Limited for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions or wish to report a problem.

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: Acetazolamide Tablets, USP (125 mg, 100-count bottle)
Variants: 125 mg, Tablet
Lot Numbers:
30575HF1 (Exp Nov 2026)
NDC:
72888-047-01

Distributed by Advagen Pharma Limited, Plainsboro, NJ. Manufactured by Rubicon Research Private Limited, Thane, India.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95217
Status: Active
Manufacturer: Rubicon Research Private Limited
Sold By: Pharmacies; Healthcare providers
Manufactured In: India
Units Affected: 3,984 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.