Device evidence

device-recall:cfres:202577

Guider Softip Guide Catheter 5F PRE-SHAPED 40 90CM, Catalog number M003100620, cardiac guide catheter

Official recall number

Z-0015-2024

Evidence summary

Product code: DQY
Recall status: Open, Classified
Event initiated: July 27, 2023
Root cause: Employee error
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-0015-2024