Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:188355

CIRCUL8 LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF: 08-0020, Rx Prescription Only, Not Sterile IP22, Latex Free,

Official recall number

Z-2324-2021

Evidence summary

Product code
JOW
Recall status
Open, Classified
Event initiated
July 09, 2021
Root cause
Unknown/Undetermined by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2324-2021

Field note

Send feedback

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