FDA Adverse Event Malfunction Summary report: N

PASSPORT 2 MONITOR

MDR report key: 3091111 · Received April 30, 2013

Report

Report Number
2221819-2013-00870
Event Type
Malfunction
Date Received
April 30, 2013
Date of Event
March 18, 2013
Report Date
April 30, 2013
Manufacturer
MINDRAY DS USA, INC.
Product Code
MHX
PMA / PMN Number
020550
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

SERVICE REPRESENTATIVE REPLACED THE UNITS MAIN BOARD AND PERFORMED FUNCTIONAL TESTS.

Description of Event or Problem · 1

CUSTOMER REPORTED AN ISSUE WITH THE PASSPORT 2 MONITOR, WHICH MAY HAVE IMPACTED ECG MONITORING. NO PT INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
187721 PASSPORT 2 MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

Patients

Seq Age Sex Outcome Treatment
1