FDA Adverse Event Malfunction Summary report: N

PASSPORT 2 MONITOR

MDR report key: 3091504 · Received April 30, 2013

Report

Report Number
2221819-2013-00348
Event Type
Malfunction
Date Received
April 30, 2013
Date of Event
August 17, 2012
Report Date
April 30, 2013
Manufacturer
MINDRAY DS USA, INC.
Product Code
MHX
PMA / PMN Number
993531
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE COMPANY REPRESENTATIVE EVALUATED THE UNIT. CORRECTIONS INCLUDED REPLACEMENT OF THE FRONT END CHIP AND CPU BOARD. THE UNIT WAS TESTED TO FACTORY'S SPECIFICATIONS.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THE PASSPORT 2 MONITOR HAD NO PARAMETERS ON THE DISPLAY, WHICH MAY HAVE RESULTED IN LOSS OF PRIMARY MONITORING. NO PATIENT INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
186412 PASSPORT 2 MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

Patients

Seq Age Sex Outcome Treatment
1