# FDA recall D-0141-2019

> **Pharm D Solutions, LLC** · Class II · drug recall initiated 2018-09-10.

## Product

Bi-Mix Injection (Alprostadil 150 mcg/Lidocaine 2 mg/mL), Pharm D Solutions, Houston, Texas --- NDC 69699-1323-05

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0141-2019
- **Recalling firm:** Pharm D Solutions, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-09-10
- **Report date:** 2018-11-07
- **Termination date:** 2021-02-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0141-2019

## Citation

> AI Analytics. FDA recall D-0141-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0141-2019. Source: US FDA. Licensed CC0.

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