D-1308-2019 Class II Terminated
FDA drug recall D-1308-2019 was initiated by Avella of Deer Valley, Inc. Store 38 on May 3, 2019 and is designated Class II. Reason for recall: Lack of assurance of sterility The recall status is terminated (terminated February 25, 2020). Affected quantity: 730 syringes.
Recall Details
- Product Type
- Drugs
- Report Date
- June 5, 2019
- Initiation Date
- May 3, 2019
- Termination Date
- February 25, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 730 syringes
Product Description
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 Pattern
U.S.A. nationwide
Code Information
Lot #: 138-20191202@64, Exp 05/13/19