AIRFLOW
Received Oct 5, 2016 · Event occurred Sep 6, 2016
Report 2246980-2016-00052 · MDR key 5999615
Device
Product problems
- Device Issue
- Separation Failure
- Device Issue
- Separation Failure
Patient
Not reported
- Not Applicable
- Missing Value Reason
- Not Applicable
- Missing Value Reason
Narrative
Additional Manufacturer Narrative
AN EXTENSIVE AND THOROUGH INVESTIGATION WAS PERFORMED BY THE ENGINEERING TEAM THAT CONCLUDED THE ROOT CAUSE FOR THIS PROBLEM IS THE FACT THAT THE PATIENT PORT AND THE MASK ARE MADE OUT OF SIMILAR BASE MATERIALS RESULTING IN AN UNDESIRABLY HIGH COEFFICIENT OF FRICTION BETWEEN THE TWO PARTS. STEPS HAVE BEEN TAKEN TO IMPLEMENT A MATERIAL COMBINATION WITH A LOWER COEFFICIENT OF FRICTION THAT SIGNIFICANTLY REDUCES THE EFFORT REQUIRED TO REMOVE THE MASK FROM THE PATIENT VALVE.
Description of Event or Problem
THE CUSTOMER ALLEGES "THE MASK COULD NOT BE REMOVED FROM THE BAG." NO OTHER DETAILS WERE PROVIDED AND NO PATIENT INJURY/HARM REPORTED.