FDA Adverse Event Malfunction Summary report: N

SECURE 2 MED/SURGBED

MDR report key: 2033191 · Received February 28, 2011

Report

Report Number
1831750-2011-01959
Event Type
Malfunction
Date Received
February 28, 2011
Date of Event
February 8, 2011
Report Date
February 8, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULT: SIDERAIL PANELS.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE RIGHT INNER AND OUTER SIDERAIL PANELS WERE CRACKED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SECURE 2 MED/SURGBED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002 NA

Patients

Seq Age Sex Outcome Treatment
1