FDA Adverse Event Malfunction Summary report: N

MA204

MDR report key: 2904448 · Received November 30, 2012

Report

Report Number
1831750-2012-12452
Event Type
Malfunction
Date Received
November 30, 2012
Date of Event
November 10, 2012
Report Date
November 10, 2012
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

LOAD CELL.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAS THE FOLLOWING ISSUES: THE POWER CORD IS MISSING THE GROUND PRONG, THE SCALE IS NOT ACCURATE, THE NURSE CALL CONNECTOR SCREWS ARE BROKEN IN THE BED. IT WAS FURTHER REPORTED THAT THE NURSE CALL CABLE WAS MISSING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MA204 A/C HOSPITAL BED FNL STRYKER MEDICAL FL25E NA

Patients

Seq Age Sex Outcome Treatment
1