FDA Adverse Event Malfunction Summary report: N

SECURE 2 MED/SURGBED

MDR report key: 2070331 · Received April 18, 2011

Report

Report Number
1831750-2011-03680
Event Type
Malfunction
Date Received
April 18, 2011
Date of Event
March 24, 2011
Report Date
March 24, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULT: POWER CORD PLUG MISSING ITS GROUND PRONG. CUT ON COMMUNICATION CORD.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE POWER CORD PLUG WAS MISSING ITS GROUND PRONG, AND THE COM CORD WAS CUT. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

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