|
Model Number 3333 |
Device Problem
Device Fell (4014)
|
Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
|
Event Date 04/01/2021 |
Event Type
malfunction
|
Manufacturer Narrative
|
This record is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program.1 device was functionally/visually inspected in the field; no defect or malfunction was found.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 experienced an unexpected drop/collapse of the seat section.There was patient involvement; no adverse consequences were reported.
|
|
Search Alerts/Recalls
|
|
|