# FDA recall D-0237-2024

> **Ascend Laboratories, LLC** · Class II · drug recall initiated 2023-12-29.

## Product

Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle, manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-626-90

## Reason for recall

Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0237-2024
- **Recalling firm:** Ascend Laboratories, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2023-12-29
- **Report date:** 2024-01-24

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0237-2024

## Citation

> AI Analytics. FDA recall D-0237-2024. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0237-2024. Source: US FDA. Licensed CC0.

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