FDA Adverse Event Malfunction Summary report: N

SM104 M-SERIES W/5TH WHEEL

MDR report key: 2113530 · Received May 24, 2011

Report

Report Number
1831750-2011-05020
Event Type
Malfunction
Date Received
May 24, 2011
Date of Event
April 26, 2011
Report Date
April 26, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

EVALUATION RESULT: FOWLER, GAS SPRING TIP.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER IS NOT GOING UP. 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 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1007 NA

Patients

Seq Age Sex Outcome Treatment
1