FDA Adverse Event Malfunction Summary report: N

3002 SECURE II

MDR report key: 2141395 · Received June 1, 2011

Report

Report Number
1831750-2011-05347
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
SC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULT: CRACKED HEAD-END LEFT SIDE RAIL PANELS.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD-END LEFT SIDERAIL, THE OUTER HOOP AND BOTH INNER AND OUTER PANELS WERE DAMAGED, AND POSSIBLY THERE WAS FLUID INTRUSION. 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