Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AngioJet AVX Thrombectomy Set: UPN 105039-001 Recalled by Boston Scientific Corporation Due to AngioJet products were distributed with an incorrect use-by...
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 Boston Scientific Corporation directly.
Affected Products
AngioJet AVX Thrombectomy Set: UPN 105039-001, Catalog No.105039, Sterilized Using Ethylene Oxide. For breaking apart and removing thrombus from vascular system, used with the AngioJet Ultra System in breaking apart and removing thrombus from A-V access conduits.
Quantity: total of 9 units
Why Was This Recalled?
AngioJet products were distributed with an incorrect use-by (expiry) date. The correct date is Nov-2015, but the units are labeled with a use-by date of Dec-2015.
Where Was This Sold?
This product was distributed to 3 states: AZ, MO, OH
About Boston Scientific Corporation
Boston Scientific Corporation has 601 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report