Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:114083

24 Fr 8mm Soft Flow Ang Wire W/L The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.

Official recall number

Z-0461-2013

Evidence summary

Product code
DWF
Recall status
Terminated
Event initiated
November 21, 2012
Root cause
Process design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0461-2013