FDA Adverse Event Malfunction Summary report: N

SAFETY NET

MDR report key: 3983574 · Received August 1, 2014

Report

Report Number
MW5037622
Event Type
Malfunction
Date Received
August 1, 2014
Date of Event
June 30, 2014
Report Date
July 31, 2014
Manufacturer
MASIMO
Product Code
MSX
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

MASIMO CORD MALFUNCTION AND NOT READING TO CENTRAL STATION, REPLACE CORD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
451792 SAFETY NET SAFETYNET MSX MASIMO

Patients

Seq Age Sex Outcome Treatment
1