Device evidence

device-recall:cfres:199403

QUADROX-iD Adult, Oxygenator used during cardiopulmonary bypass Model Item No. HMOD 70000-USA 701067840 BEQ-HMOD70000-USA 701067859

Official recall number

Z-1656-2023

Evidence summary

Product code: DTZ
Recall status: Open, Classified
Event initiated: May 18, 2023
Root cause: Under Investigation by firm
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1656-2023