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

Votrient (pazopanib) Tablets Recalled for Failed Dissolution

Agency Publication Date: December 13, 2023
Share:
Sign in to monitor this recall

Summary

Siegfried Barbera, SL is recalling approximately 2,016 bottles of Votrient (pazopanib) 200 mg tablets because the product failed dissolution testing. This medication, distributed by Novartis Pharmaceuticals Corp., is packaged in 120-count bottles. This defect means the tablets may not break down correctly in the body, which could potentially interfere with how the medication is absorbed. No incidents or injuries have been reported to date.

Risk

If the tablets fail to dissolve as specified, the patient may not receive the full intended dose of the medication, which could reduce its effectiveness in treating the underlying condition.

What You Should Do

  1. This recall affects Votrient (pazopanib) 200 mg tablets sold in 120-count bottles with NDC 0078-1077-66.
  2. Identify affected products by checking for lot number ME2713 (Expiration 02/2025), or lot numbers MF8286 and ML1860 (Expiration 04/2025).
  3. 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 the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for more information.

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: Votrient (pazopanib) (200 mg, 120-count bottle)
Variants: 200 mg, 120-count bottle, Tablet
Lot Numbers:
ME2713 (Exp. 02/2025)
MF8286 (Exp. 04/2025)
ML1860 (Exp. 04/2025)
NDC:
0078-1077-66

Distributed by Novartis Pharmaceuticals Corp.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93429
Status: Resolved
Manufacturer: Siegfried Barbera, SL
Sold By: Novartis Pharmaceuticals Corp.
Manufactured In: Spain
Units Affected: 2016
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.