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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:142937

Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This instrument has been designed to be used with an Olympus video system center, light source, documentation equipment, monitors, EndoTherapy accessories, and other ancillary equipment for endoscopy and endoscopic surgery within the duodenum.

Official recall number

Z-0757-2016

Evidence summary

Product code
FDT
Recall status
Terminated
Event initiated
January 08, 2016
Root cause
No Marketing Application
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0757-2016

Field note

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