# FDA recall D-0998-2020

> **Mayne Pharma Inc** · Class II · drug recall initiated 2020-03-02.

## Product

Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01

## Reason for recall

Product Mix-Up: A foreign tablet was found in bottle.

## Distribution

Distributed Nationwide in the USA

## Key facts

- **Recall number:** D-0998-2020
- **Recalling firm:** Mayne Pharma Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2020-03-02
- **Report date:** 2020-03-18
- **Termination date:** 2021-10-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Greenville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0998-2020

## Citation

> AI Analytics. FDA recall D-0998-2020. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0998-2020. Source: US FDA. Licensed CC0.

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