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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:139223

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.

Official recall number

Z-2380-2015

Evidence summary

Product code
DXE
Recall status
Terminated
Event initiated
July 31, 2015
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2380-2015

Field note

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