Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:200791

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780080

Official recall number

Z-1948-2023

Evidence summary

Product code
BTR
Recall status
Open, Classified
Event initiated
May 25, 2023
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1948-2023

Field note

Send feedback

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