FDAFDA · Food and drugs·Recall number D-0224-2019
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
Published November 14, 2018 · Recall initiated: October 31, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Avella of Deer Valley, Inc. Store 38
- Distributor
- Product was distributed throughout the United States.
- Lot
- Lot # 138-20182408@58 BUD 12/22/2018
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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