Model Number 8300 |
Device Problems
Failure to Calibrate (2440); Calibration Problem (2890); Appropriate Term/Code Not Available (3191)
|
Patient Problems
No Patient Involvement (2645); No Clinical Signs, Symptoms or Conditions (4582)
|
Event Type
malfunction
|
Manufacturer Narrative
|
Although requested, device has not been received.A follow up report will be submitted with failure investigation results should the device be received for evaluation.
|
|
Event Description
|
It was reported that the device received an unknown error while performing co2 sensor calibration.No additional information was provided.There was no patient involvement.
|
|
Event Description
|
It was reported that the device received an unknown error while performing co2 sensor calibration.No additional information was provided.There was no patient involvement.
|
|
Manufacturer Narrative
|
The investigation is pending.A follow up report will be submitted once the failure investigation has been completed.
|
|
Manufacturer Narrative
|
This device was evaluated and repaired through the service repair process.Upon visual inspection the service technician noted that they error code 570.6200 was confirmed due to a bad oridion board that failed co2 calibration.Replaced it a new oridion board.Performed leak down test and co2 calibration with passing results.A review of the device history record showed the device had a manufacture date of 22oct2018.The review was performed from the date of manufacture to the date of product release for distribution.A review of the device history record in sap for sn (b)(6), was performed which confirmed that this device was not involved in a production failure which correlates to the customer reported issue.Based on the findings, service determined that the proximate cause of the reported issue was due to electrical failure of the oridion assy board etco2 v1 rohs.A review of the complaint history record in trackwise and sap was performed for the sn (b)(6) which did not confirm similar complaints with the same or related failure mode for this customer.
|
|
Event Description
|
It was reported that the device received an unknown error while performing co2 sensor calibration.No additional information was provided.There was no patient involvement.
|
|
Search Alerts/Recalls
|