Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:182027

Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 35cc IAB (Japan) Kit P/N: 0684-00-0607 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Failure.

Official recall number

Z-2843-2020

Evidence summary

Product code
DSP
Recall status
Open, Classified
Event initiated
July 27, 2020
Root cause
Process change control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2843-2020