FDA Adverse Event Malfunction Summary report: N

PASSPORT V MONITOR

MDR report key: 3091261 · Received April 30, 2013

Report

Report Number
2221819-2013-00538
Event Type
Malfunction
Date Received
April 30, 2013
Date of Event
February 5, 2013
Report Date
April 30, 2013
Manufacturer
MINDRAY DS USA, INC.
Product Code
MHX
PMA / PMN Number
091834
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

MINDRAY SERVICES REPS FOUND POWER SUPPLY WAS DISCONNECTED AND A BATTERY ISSUE FURTHER CONTRIBUTING TO THE SHUT DOWN. ISSUES WERE CORRECTED AND UNIT WAS TESTED TO FACTORY SPECIFICATIONS.

Description of Event or Problem · 1

CUSTOMER REPORTED THE PASSPORT V MONITOR SHUT DOWN WHICH MAY HAVE RESULTED IN A LOSS OF PRIMARY MONITORING. NO PT INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
186364 PASSPORT V MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

Patients

Seq Age Sex Outcome Treatment
1