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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:197166

Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400F (IPN000306), cardiac pump

Official recall number

Z-0445-2023

Evidence summary

Product code
DSP
Recall status
Open, Classified
Event initiated
October 17, 2022
Root cause
Pending
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0445-2023