FDA Adverse Event Malfunction Summary report: N

SECURE II MED/SURG BED

MDR report key: 2021473 · Received February 16, 2011

Report

Report Number
1831750-2011-01457
Event Type
Malfunction
Date Received
February 16, 2011
Date of Event
January 26, 2011
Report Date
January 26, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

SIDERAIL OUTER PANELS.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE SIDERAILS ARE CRACKED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1