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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:199910

Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Model Number 0998-00-0800-55, Part Number 0998-00-0800-XX

Official recall number

Z-1907-2023

Evidence summary

Product code
DSP
Recall status
Open, Classified
Event initiated
May 04, 2023
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1907-2023

Field note

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