FDA Adverse Event Malfunction Summary report: N

RENAISSANCE 26 STRETCHER

MDR report key: 2051477 · Received April 4, 2011

Report

Report Number
1831750-2011-03268
Event Type
Malfunction
Date Received
April 4, 2011
Date of Event
March 7, 2011
Report Date
March 7, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKE WAS BROKEN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RENAISSANCE 26 STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1211 NA

Patients

Seq Age Sex Outcome Treatment
1 NA