Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:195615

BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70106.9078. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.

Official recall number

Z-1767-2022

Evidence summary

Product code
DTZ
Recall status
Open, Classified
Event initiated
July 22, 2022
Root cause
Package design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1767-2022