FDA Adverse Event Malfunction Summary report: N

SECURE ACUTE CARE BED

MDR report key: 2143725 · Received June 3, 2011

Report

Report Number
1831750-2011-05451
Event Type
Malfunction
Date Received
June 3, 2011
Date of Event
May 9, 2011
Report Date
May 9, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

RESULT: MOUNTING BRACKET, GLIDE ROD.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE SIDERAIL HAD FALLEN OFF. IT IS UNK IF THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SECURE ACUTE CARE BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3000 NA

Patients

Seq Age Sex Outcome Treatment
1