FDA Adverse Event Malfunction Summary report: N

V60 VENTILATOR

MDR report key: 4090277 · Received September 15, 2014

Report

Report Number
2031642-2014-01039
Event Type
Malfunction
Date Received
September 15, 2014
Report Date
August 18, 2014
Manufacturer
RESPIRONICS CALIFORNIA, INC.
Product Code
MNT
PMA / PMN Number
K082660
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 1

RECEIVED BY MFR DATE: 10/24/2014. CONCLUSION / ROOT CAUSE: THE GAS DELIVERY SYSTEM ASSEMBLY WAS TESTED AND NO FAILURES WERE IDENTIFIED. THE REPORTED ERROR CODES COULD NOT BE DUPLICATED. THIS REPORT IS BEING SUBMITTED AS PART OF THE REMEDIATION FOR CAPA (B)(4).

Additional Manufacturer Narrative · 1

GAS DELIVERY SYSTEM.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THE VENTILATOR ALARMED DUE TO A VENT INOP OCCURRENCE. THE CUSTOMER REPORTED THE UNIT WAS NOT IN USE ON A PATIENT THEREFORE THERE WAS NO PATIENT INVOLVEMENT OR HARM. THE MANUFACTURERS FIELD SERVICE ENGINEER (FSE) WAS UNABLE TO DUPLICATE THE REPORTED PROBLEM. THE FSE REPORTED REVIEW OF THE DEVICE DIAGNOSTIC HISTORY NOTED A DATA ACQUISITION PCBA ADC FAILURE WHICH MAY RESULT IN A VENT INOP OCCURRENCE. A VENT INOP CONDITION DURING OPERATION WILL RESULT IN A VISUAL AND AUDIBLE ALARM AND PRECLUDES CONTINUED SAFE OPERATION OF THE VENTILATOR. THE USER MUST PROVIDE ALTERNATIVE VENTILATION AND HAVE THE VENTILATOR SERVICED. THE FSE REPLACED THE GAS DELIVERY SYSTEM TO ADDRESS THE FINDINGS AND REPORTED PROBLEM. APPLICABLE FINAL TESTING WAS PERFORMED PER OPERATING SPECIFICATIONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
568411 V60 VENTILATOR VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE MNT RESPIRONICS CALIFORNIA, INC. V60 NA

Patients

Seq Age Sex Outcome Treatment
1