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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:213384

INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.

Official recall number

Z-1724-2025

Evidence summary

Product code
KTI
Recall status
Open, Classified
Event initiated
April 04, 2025
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1724-2025

Field note

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