FDA Adverse Event Malfunction Summary report: N

SERVO-S

MDR report key: 2223465 · Received June 17, 2011

Report

Report Number
8010042-2011-00107
Event Type
Malfunction
Date Received
June 17, 2011
Date of Event
July 10, 2009
Report Date
May 20, 2011
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
CBK
PMA / PMN Number
K041223
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THE RETURNED AIR GAS MODULE WHICH REGULATES THE INSPIRATORY AIR GAS FLOW TO THE PT WAS INVESTIGATED. THE REPORTED PRESSURE TRANSDUCER TEST FAILURE DURING PRE-USE CHECK WAS REPRODUCED. THE TESTS PERFORMED ON THE AIR GAS MODULE REVEALED THAT THE MEMBRANE IN THE NOZZLE UNIT MOUNTED IN THE GAS MODULE WAS STICKY. THE NOZZLE UNIT, WHICH IS PART OF THE GAS MODULE AND CONSISTS OF A MEMBRANE, A MOUTHPIECE AND A FEATHER SPRING, IS USED FOR REGULATION OF THE GAS FLOW THROUGH THE GAS MODULE. THE MEMBRANE IN THE NOZZLE UNIT IS PRESSED AGAINST A MOUTHPIECE WITH A FEATHER SPRING TO REGULATE THE GAS FLOW THROUGH THE GAS MODULE. THE MEMBRANE STICKINESS MAY CAUSE THE FEATHER SPRING TO GET STUCK TO THE MEMBRANE WHILE BEING PRESSED ONTO IT AND THUS CAUSING A DELAY ON RELEASE. THE DELAY AFFECTS THE REGULATION OF THE GAS FLOW THROUGH THE GAS MODULE AND CAUSES FAILURE DURING PRE-USE CHECK AND, DURING VENTILATION, CAUSES THE DELIVERED GAS FLOW AND PRESSURE TO BE HIGHER THAN SET. A FEATHER SPRING WITH A COARSE SURFACE WAS INTRODUCED IN (B)(6) 2010 TO PREVENT IT FROM GETTING STUCK TO THE MEMBRANE. THE CAUSE OF THE STICKINESS IS WEAR OF THE MEMBRANE IN NOZZLE UNIT. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE VENTILATOR FAILED PRESSURE TRANSDUCER TEST DURING PRE-USE CHECK. (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SERVO-S CBK MAQUET CRITICAL CARE AB

Patients

Seq Age Sex Outcome Treatment
1