# FDA recall D-0224-2019

> **Avella of Deer Valley, Inc. Store 38** · Class II · drug recall initiated 2018-10-31.

## Product

BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG in normject syringe) Repackaged by Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix, AZ 85085. NDC 42852-001-24

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Product was distributed throughout the United States.

## Key facts

- **Recall number:** D-0224-2019
- **Recalling firm:** Avella of Deer Valley, Inc. Store 38
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-10-31
- **Report date:** 2018-11-14
- **Termination date:** 2019-01-18

- **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-0224-2019

## Citation

> MORVS. FDA recall D-0224-2019. Retrieved 2026-10-15 from https://api.morvs.ai/recall/D-0224-2019. Source: US FDA. Licensed CC0.

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