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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:186140

Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provides temporary support to the left ventricle via the principle of counterpulsation, Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85

Official recall number

Z-1507-2021

Evidence summary

Product code
DSP
Recall status
Open, Classified
Event initiated
March 22, 2021
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1507-2021

Field note

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