FDA Adverse Event Malfunction Summary report: N

SM204 M-SERIES W/BIG WHEEL

MDR report key: 2143579 · Received June 2, 2011

Report

Report Number
1831750-2011-05437
Event Type
Malfunction
Date Received
June 2, 2011
Date of Event
May 5, 2011
Report Date
May 5, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

EVALUATION RESULT: GAS SPRING TRIP, FOWLER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BED WAS BROKEN. THE HEAD WOULD NOT LIFT. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SM204 M-SERIES W/BIG WHEEL HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1015 NA

Patients

Seq Age Sex Outcome Treatment
1