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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:181531

Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE, Product Code IAP-0500

Official recall number

Z-2410-2020

Evidence summary

Product code
DSP
Recall status
Terminated
Event initiated
May 20, 2020
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2410-2020

Field note

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