FDA recall D-0224-2019

Avella of Deer Valley, Inc. Store 38 · Class II · drug

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

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

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0224-2019