Catalog Number 6252000000 |
Device Problems
Difficult or Delayed Positioning (1157); Device Fell (4014)
|
Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
|
Event Date 07/01/2020 |
Event Type
malfunction
|
Manufacturer Narrative
|
This mdr is part of the fda voluntary malfunction summary reporting program.The device was evaluated in the field and the issue was confirmed; there were broken/damaged components.The device was repaired and returned.There was no remedial action taken.This device is not labeled for single use.
|
|
Event Description
|
This report summarizes 1 malfunction event, where it was reported the device collapsed/dropped and it was difficult to maneuver.There was no patient involvement.
|
|
Search Alerts/Recalls
|