Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:196522

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT 2 IAPB, REF IAP-0400 (IPN000302), cardiac pump

Official recall number

Z-0426-2023

Evidence summary

Product code
DSP
Recall status
Open, Classified
Event initiated
October 17, 2022
Root cause
Pending
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0426-2023