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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.

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Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

Nebivolol 20 mg Tablets Recalled for Product Cross Contamination

Agency Publication Date: December 9, 2025
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Summary

Glenmark Pharmaceuticals Inc., USA is recalling 672 bottles of Nebivolol (20 mg) tablets, a prescription medication used to treat high blood pressure. The recall was initiated because the tablets may have been cross-contaminated with other products during the manufacturing process. These products were distributed nationwide in 90-count bottles under the Avkare brand.

Risk

Cross-contamination can introduce unintended active pharmaceutical ingredients into the medication, which may lead to unpredictable side effects or adverse drug reactions.

What You Should Do

  1. Check your medication bottle for Nebivolol Tablets, 20 mg (90-count) with NDC 42291-874-90, Lot number 17240988, and an expiration date of 05/31/2026.
  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 Glenmark Pharmaceuticals Inc., USA 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: Nebivolol Tablets (90 Tablets)by Avkare
Variants: 20 mg, Rx Only
Lot Numbers:
17240988 (Exp. 05/31/2026)
NDC:
42291-874-90

Manufactured for Avkare, Pulaski, TN; Manufactured by Glenmark Pharmaceuticals Limited, India.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98014
Status: Active
Manufacturer: Glenmark Pharmaceuticals Inc., USA
Sold By: Avkare
Manufactured In: India, Italy
Units Affected: 672 90-count 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.