FDA Adverse Event Malfunction Summary report: N

V60 VENTILATOR

MDR report key: 6089462 · Received November 9, 2016

Report

Report Number
2031642-2016-03046
Event Type
Malfunction
Date Received
November 9, 2016
Report Date
October 14, 2016
Manufacturer
RESPIRONICS CALIFORNIA, INC
Product Code
MNT
PMA / PMN Number
K082660
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NV, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

UPDATED.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THE FAILED BATTERY TEST . NO PATIENT INVOLVEMENT REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
742592 V60 VENTILATOR VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE MNT RESPIRONICS CALIFORNIA, INC V60

Patients

Seq Age Sex Outcome Treatment
1