# FDA recall D-0940-2023

> **SUN PHARMACEUTICAL INDUSTRIES INC** · Class II · drug recall initiated 2023-07-13.

## Product

Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, NDC 57664-230-88.

## Reason for recall

Presence of Foreign Substance: Metal embedded in a tablet.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0940-2023
- **Recalling firm:** SUN PHARMACEUTICAL INDUSTRIES INC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-07-13
- **Report date:** 2023-08-02
- **Termination date:** 2024-02-12

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0940-2023

## Citation

> AI Analytics. FDA recall D-0940-2023. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/D-0940-2023. Source: US FDA. Licensed CC0.

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