Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:177530

CS5/5+ Fastpacks, 125 mL, 20¿ Res Autotransfusion Device- Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.

Official recall number

Z-0889-2020

Evidence summary

Product code
CAC
Recall status
Terminated
Event initiated
October 21, 2019
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0889-2020

Field note

Send feedback

We'll only use this to respond to your feedback.