FDA Adverse Event Malfunction Summary report: N

SM104 M-SERIES W/5TH WHEEL

MDR report key: 2191611 · Received July 1, 2011

Report

Report Number
1831750-2011-06690
Event Type
Malfunction
Date Received
July 1, 2011
Date of Event
June 6, 2011
Report Date
June 6, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

RESULT: SPRING SPACER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE RIGHT SIDE RAIL WILL NOT STAY LOCKED IN THE UP POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SM104 M-SERIES W/5TH WHEEL WHEELED STRETCHER FPO STRYKER MEDICAL 1007 NA

Patients

Seq Age Sex Outcome Treatment
1