Device evidence

device-recall:cfres:208195

This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then inserted into the cannula. Catalog Number: 0406-630-225

Official recall number

Z-2261-2024

Evidence summary

Product code: GXI
Recall status: Open, Classified
Event initiated: June 03, 2024
Root cause: Storage
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-2261-2024