# FDA recall D-0918-2018

> **SCA Pharmaceuticals** · Class II · drug recall initiated 2018-06-29.

## Product

Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total Volume, Rx only , SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205 877-550-5059

## Reason for recall

Subpotent Drug: Stability data does not support the current expiration dating of 55 days after compounding.

## Distribution

United States

## Key facts

- **Recall number:** D-0918-2018
- **Recalling firm:** SCA Pharmaceuticals
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-06-29
- **Report date:** 2018-07-18
- **Termination date:** 2019-05-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Little Rock, AR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0918-2018

## Citation

> AI Analytics. FDA recall D-0918-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0918-2018. Source: US FDA. Licensed CC0.

---

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