Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:196175

Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP 120807FP Fogarty Arterial Embolectomy Catheter with Stylet Model Number: 120403FSP 120803FSP

Official recall number

Z-0146-2023

Evidence summary

Product code
DXE
Recall status
Open, Classified
Event initiated
October 06, 2022
Root cause
Packaging
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0146-2023