FDA Adverse Event Malfunction Summary report: N

PASSPORT 2 MONITOR

MDR report key: 3091242 · Received April 30, 2013

Report

Report Number
2221819-2013-00626
Event Type
Malfunction
Date Received
April 30, 2013
Date of Event
February 19, 2013
Report Date
April 30, 2013
Manufacturer
MINDRAY DS USA, INC.
Product Code
DSI
PMA / PMN Number
993531
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

MINDRAY SERVICE REPRESENTATIVE REPLACED THE POWER SUPPLY AND ENCODER. CALIBRATED AND SAFETY TESTED UNIT TO FACTORY SPECIFICATIONS.

Description of Event or Problem · 1

CUSTOMER REPORTED THE PASSPORT 2 MONITOR SHUT DOWN WHICH MAY HAVE RESULTED IN A LOSS OF MONITORING. NO PT INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
187592 PASSPORT 2 MONITOR PATIENT MONITOR DSI MINDRAY DS USA, INC.

Patients

Seq Age Sex Outcome Treatment
1