Glenmark Pharmaceuticals recalls 20 mg Nebivolol tablets due to cross contamination risk. Affected lots manufactured in India with specific expiration date. Consumers should check product details and contact for guidance.
Cross Contamination with Other Products
Glenmark is recalling 20 mg Nebivolol tablets that may have cross-contaminated with other products. This could affect people taking blood pressure medication, but the recall does not specify a risk of serious injury.
Cross contamination means the tablets might contain other products unintentionally. This could lead to unintended medication effects, but the recall does not specify serious injury risks.
People who have prescription Nebivolol tablets from this specific lot number. Those with blood pressure conditions are most at risk if the tablets are contaminated.
Check for the lot number 17240988 on the packaging. The tablets were manufactured in India with an expiration date of May 31, 2026.
Look for the lot number 17240988 on the packaging to confirm if your tablets are affected.
The recall is due to cross contamination with other products, which could affect medication safety.
Check the lot number on the packaging. If it matches 17240988, contact Glenmark for further instructions.
The recall does not specify a risk of serious injury, so the danger level is low risk.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0222-2026 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0222-2026 from Glenmark. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
