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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:209208

Avance CS2 and Avance CS2 Pro. These anesthesia gas machines are intended to provide general inhalation anesthesia and ventilatory support to patients and are to be used only by medical professionals trained and qualified in the administration of general anesthesia.

Official recall number

Z-0080-2025

Evidence summary

Product code
BSZ
Recall status
Open, Classified
Event initiated
July 12, 2024
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0080-2025

Field note

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