Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:149494

LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation System is intended for use by physicians as a prescription device for the application of localized heat and pressure therapy in adult patients with chronic cystic conditions of the eyelids, including meibomian gland dysfunction (MGD), also known as evaporative dry eye or lipid deficiency dry eye.

Official recall number

Z-0093-2017

Evidence summary

Product code
ORZ
Recall status
Terminated
Event initiated
September 13, 2016
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0093-2017

Field note

Send feedback

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