Glenmark Pharmaceuticals recalled 672 bottles of Nebivolol Tablets on November 18, 2025, due to cross-contamination. The 20 mg tablets, prescribed for hypertension, may pose health risks. Consumers should stop using the product and seek guidance from healthcare providers.
Cross Contamination with Other Products
Consumers and healthcare providers should stop using this product immediately. Contact Glenmark Pharmaceuticals Inc., USA or your healthcare provider for guidance. Notification method: Letter
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Nebivolol is a medication used to treat high blood pressure and heart conditions. It is typically prescribed for hypertension management and can help lower the risk of heart-related issues.
The recall was initiated due to cross-contamination with other products, which can compromise the safety and effectiveness of the medication.
This recall is not part of a broader industry pattern.
Consumers should stop using the product to avoid potential health risks. This recall may cause inconvenience for those relying on the medication.
Lot numbers and expiration dates are typically printed on the medicine bottle label.
Refund processing can take approximately 4-6 weeks after returning the product.
Keep receipts, correspondence regarding the recall, and any evidence of the product for your records.
The recall involves Nebivolol Tablets, 20 mg, sold in 90-count bottles. The products were manufactured by Glenmark Pharmaceuticals Limited in India for Avkare, Pulaski, TN. The affected lot number is 17240988, with an expiration date of May 31, 2026.
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