FDA recall D-1308-2019
Avella of Deer Valley, Inc. Store 38 · Class II · drug
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
- 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
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1308-2019