# FDA recall D-0654-2024

> **ProRx LLC** · Class II · drug recall initiated 2024-08-22.

## Product

Semaglutide / Cyanocobalamin Injection:  2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX 267-565-7008, NDC 84139-225-02

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0654-2024
- **Recalling firm:** ProRx LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-08-22
- **Report date:** 2024-09-11

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0654-2024

## Citation

> AI Analytics. FDA recall D-0654-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-0654-2024. Source: US FDA. Licensed CC0.

---

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