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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:184211

Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog Number: 06597035 UPN: H787065970355

Official recall number

Z-0418-2021

Evidence summary

Product code
DQR
Recall status
Terminated
Event initiated
October 14, 2020
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0418-2021

Field note

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