Catalog Number 6500000000 |
Device Problems
Positioning Failure (1158); Device Fell (4014)
|
Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
|
Event Date 07/01/2023 |
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.The device was repaired and returned to use.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 cot height cannot be adjusted and unintended cot lowering or cot dropping to lowest position (no cot tip).There was no patient involvement.
|
|
Search Alerts/Recalls
|