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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:110339

System 1 Base 100/120V The Terumo Advanced Perfusion System 1 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical professional who is experienced in the operation of this or similar equipment.

Official recall number

Z-1968-2012

Evidence summary

Product code
DTQ
Recall status
Terminated
Event initiated
June 25, 2012
Root cause
Equipment maintenance
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1968-2012

Field note

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