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

FDA recall notice · announced November 14, 2018 · Avella Of Deer Valley, Inc. Store 38

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The 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

Notes

Distribution: Product was distributed throughout the United States.
Lot/code information: Lot # 138-20182408@58 BUD 12/22/2018
Quantity: 911 syringes
Status: Terminated
Products in this recall event:
- 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 (D-0224-2019)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.