D-1058-2013 Class II Terminated

Recalled by Avella of Deer Valley, Inc. — Phoenix, AZ

FDA drug recall D-1058-2013 was initiated by Avella of Deer Valley, Inc. on September 9, 2013 and is designated Class II. Reason for recall: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling bevacizumab and vancomycin due to concerns of sterility assurance with the specialty pharmacy's independent testing laboratory. The recall status is terminated (terminated October 17, 2013). Affected quantity: 750 units.

Recall Details

Product Type
Drugs
Report Date
September 25, 2013
Initiation Date
September 9, 2013
Termination Date
October 17, 2013
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
750 units

Product Description

Bevacizumab 1.25 mg/0.05 mL PF, Avella Specialty Pharmacy, Phoenix, AZ, 85085, 877-782-7684

Reason for Recall

Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling bevacizumab and vancomycin due to concerns of sterility assurance with the specialty pharmacy's independent testing laboratory.

Distribution Pattern

Nationwide and Puerto Rico

Code Information

12-20130508@179, Exp 11/3/2013