Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:197192

Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85, 0998-UC-0800-75, 0998-UC-0800-83, 0998-UC-0800-85.

Official recall number

Z-0886-2023

Evidence summary

Product code
DSP
Recall status
Open, Classified
Event initiated
December 19, 2022
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0886-2023