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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:142560

GE Healthcare, Aisys, 1011-9000-000. The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). The device is intended for volume or pressure control ventilation. The Aisys is not suitable for use in a MRI environment.

Official recall number

Z-0680-2016

Evidence summary

Product code
BSZ
Recall status
Terminated
Event initiated
December 15, 2015
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0680-2016

Field note

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