|
Model Number 4402 |
Device Problem
Material Integrity Problem (2978)
|
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 not evaluated, as the issue was identified and resolved during a troubleshooting call between the customer and stryker technical support.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 a broken tub.There was no patient involvement.
|
|
Search Alerts/Recalls
|
|
|