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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:182450

Flexible Intubation Video Endoscope, Part: 11302BDX, with Instruction Manual: Z18443US - Product Usage: are intended to be used for examination and visualization of a patient s upper airway and for aiding placement of an endotracheal tube.

Official recall number

Z-2896-2020

Evidence summary

Product code
CAL
Recall status
Open, Classified
Event initiated
July 27, 2020
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2896-2020