# FDA recall D-0154-2020

> **Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center** · Class III · drug recall initiated 2019-10-21.

## Product

PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL pre-filled syringes, Nephron 503B Outsourcing Facility 4500 12th St. Ext West Columbia, SC 29172, NDC 69374-919-10.

## Reason for recall

Incorrect labeling: Incorrect or missing lot and/or exp date

## Distribution

Nationwide in the U.S.

## Key facts

- **Recall number:** D-0154-2020
- **Recalling firm:** Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-10-21
- **Report date:** 2019-11-06
- **Termination date:** 2020-05-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** West Columbia, SC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0154-2020

## Citation

> AI Analytics. FDA recall D-0154-2020. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-0154-2020. Source: US FDA. Licensed CC0.

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