# FDA recall D-0142-2020

> **KVK-Tech, Inc.** · Class III · drug recall initiated 2019-10-04.

## Product

Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown, PA 18940, NDC 10702-0163-50.

## Reason for recall

Presence of Foreign Substance; Fiber particles.

## Distribution

Nationwide in the U.S.

## Key facts

- **Recall number:** D-0142-2020
- **Recalling firm:** KVK-Tech, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-10-04
- **Report date:** 2019-10-23
- **Termination date:** 2020-04-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Newtown, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0142-2020

## Citation

> AI Analytics. FDA recall D-0142-2020. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/D-0142-2020. Source: US FDA. Licensed CC0.

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