# FDA recall D-1308-2019

> **Avella of Deer Valley, Inc. Store 38** · Class II · drug recall initiated 2019-05-03.

## Product

Bevacizumab 2.5 mg/0.1 mL, packaged in a Prefilled Syringe, Rx only, AVELLA SPECIALTY PHARMACY 24416 N. 19TH AVENUE PHOENIX, AZ 85085, NDC 42852-001-27

## Reason for recall

Lack of assurance of sterility

## Distribution

U.S.A. nationwide

## Key facts

- **Recall number:** D-1308-2019
- **Recalling firm:** Avella of Deer Valley, Inc. Store 38
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-05-03
- **Report date:** 2019-06-05
- **Termination date:** 2020-02-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Phoenix, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1308-2019

## Citation

> AI Analytics. FDA recall D-1308-2019. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/D-1308-2019. Source: US FDA. Licensed CC0.

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