Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:123807

Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. " Examination and treatment of the tracheobronchial tree Contraindications for Bronchoscopy " Uncontrolled angina, uncontrolled heart failure, or serious uncontrolled ventricular arrhythmias " Uncontrolled hypertension " Bleeding disorder or use of anticoagulants.

Official recall number

Z-0527-2014

Evidence summary

Product code
ECQ
Recall status
Terminated
Event initiated
November 13, 2013
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0527-2014

Field note

Send feedback

We'll only use this to respond to your feedback.