inforMED
MalfunctionBTM

AIRFLOW

Received Oct 5, 2016 · Event occurred Sep 6, 2016

Report 2246980-2016-00052 · MDR key 5999615

Device

Generic name

Resus Bag

Manufacturer

Ventlab Llc.

Model number

AF1100MB-MMC

Lot number

305202

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.