Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bevacizumab 2.5 mg/0.1 mL Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of assurance of sterility
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Avella of Deer Valley, Inc. Store 38 directly.
Affected Products
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
Quantity: 730 syringes
Why Was This Recalled?
Lack of assurance of sterility
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Avella of Deer Valley, Inc. Store 38
Avella of Deer Valley, Inc. Store 38 has 50 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report