Device evidence

device-recall:cfres:141784

LeMaitre Single Lumen Embolectomy Catheter 3F, 80 cm, Model 1601-38 and e1601-38. Indicated for the removal of arterial emboli and thrombi.

Official recall number

Z-0386-2016

Evidence summary

Product code: DXE
Recall status: Terminated
Event initiated: October 21, 2015
Root cause: Packaging process control
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-0386-2016