# FDA recall D-0222-2026

> **Glenmark Pharmaceuticals Inc., USA** · Class III · drug recall initiated 2025-11-18.

## Product

Nebivolol Tablets, 20 mg, 90 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for Avkare, Pulaski, TN 38478, Product of Italy, NDC 42291-874-90.

## Reason for recall

Cross Contamination with Other Products

## Distribution

U.S. Nationwide

## Key facts

- **Recall number:** D-0222-2026
- **Recalling firm:** Glenmark Pharmaceuticals Inc., USA
- **Classification:** Class III
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2025-11-18
- **Report date:** 2025-12-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mahwah, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0222-2026

## Citation

> AI Analytics. FDA recall D-0222-2026. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-0222-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*