May 2019 FDA Recall Drug by Avella Of Deer Valley, Inc. Store 38
D-1308-2019 - Lack of assurance of sterility

This Class II drug recall was voluntarily initiated by Avella Of Deer Valley, Inc. Store 38 on May 3, 2019 for the product Drug. The FDA reported the reason for recall as lack of assurance of sterility. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1308-2019

Reason for Recall
Lack of assurance of sterility
Initiated
05-03-2019
Reported
06-05-2019
Quantity
730 syringes

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Avella of Deer Valley, Inc. Store 38
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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

Batch or Lot Expiration Information

Lot# : 138-20191202@64, Exp 05/13/19