FDA Adverse Event Malfunction Summary report: N

TRIO MOBILE SURGY PLTFRM 2/08

MDR report key: 2000196 · Received February 3, 2011

Report

Report Number
1831750-2011-01005
Event Type
Malfunction
Date Received
February 3, 2011
Date of Event
January 5, 2011
Report Date
January 5, 2011
Manufacturer
STRYKER MEDICAL
Product Code
INK
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER DRIFTS DOWN WITH WEIGHT. IT IS UNK IF THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRIO MOBILE SURGY PLTFRM 2/08 HOSPITAL WHEELED STRETCHER INK STRYKER MEDICAL 1033 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK