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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:203717

Tracheal fiberscope-airway management, which includes observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: LF-DP, LF-GP, LF-TP.

Official recall number

Z-0338-2024

Evidence summary

Product code
EOQ
Recall status
Open, Classified
Event initiated
September 25, 2023
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0338-2024

Field note

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