Avella of Deer Valley, Inc. Store 38 recalls Bevacizumab 2.5 mg/0.1 mL, packaged in a Prefilled Syringe, Rx only, AVELLA SPECIALTY PHARMACY 24416 N. 19TH AVENUE PHOE
Recalled June 5, 2019 · FDA recall D-1308-2019 · Avella of Deer Valley, Inc. Store 38
Hazard
Lack of assurance of sterility · FDA Class II
Units
730 syringes
Sold at
U.S.A. nationwide
Description
Lack of assurance of sterility
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
Manufacturer(s)
Avella of Deer Valley, Inc. Store 38
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →