FDA Adverse Event Malfunction Summary report: N

3002 SECURE II

MDR report key: 2141397 · Received June 1, 2011

Report

Report Number
1831750-2011-05345
Event Type
Malfunction
Date Received
June 1, 2011
Date of Event
May 4, 2011
Report Date
May 4, 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: CRACKED HEAD LEFT SIDERAIL PANEL.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD LEFT SIDERAIL PANEL WAS CRACKED, WITH FLUID INTRUSION, BUT NO ELECTRICAL SHORTS OCCURRED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1