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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:108874

SARNS FLEXIBLE ARTERIAL CANNULA: 7.3 MM (22 FR) 00 WITH 3/8" CONNECTOR,SUTURE RING, 9.5" (24 CM) LONG. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

Official recall number

Z-1836-2012

Evidence summary

Product code
DWF
Recall status
Terminated
Event initiated
May 09, 2012
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1836-2012

Field note

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