FDA Adverse Event Malfunction Summary report: N

ADVANTAGE SERIES 26 OBS

MDR report key: 2120023 · Received May 26, 2011

Report

Report Number
1831750-2011-05123
Event Type
Malfunction
Date Received
May 26, 2011
Date of Event
April 28, 2011
Report Date
April 28, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

RESULT: SPINDLE.

Description of Event or Problem · 1

IT WAS REPORTED BY SVC REPORT THAT THE STRETCHER HAS A BROKEN WELD ON THE SPINDLE FOR THE SIDE RAIL. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ADVANTAGE SERIES 26 OBS STRETCHER, WHEELED FPO STRYKER MEDICAL 1001 NA

Patients

Seq Age Sex Outcome Treatment
1