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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:199397

BEQ-HMO 50000-USA/ QUADROX-i Small, Oxygenator used during cardiopulmonary bypass Item no. 701067905

Official recall number

Z-1636-2023

Evidence summary

Product code
DTZ
Recall status
Open, Classified
Event initiated
May 18, 2023
Root cause
Pending
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1636-2023

Field note

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