FDA Adverse Event Malfunction Summary report: N

IN TOUCH ZU

MDR report key: 2133201 · Received May 4, 2011

Report

Report Number
1831750-2011-04289
Event Type
Malfunction
Date Received
May 4, 2011
Date of Event
April 5, 2011
Report Date
April 5, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

ELECTRICAL PROBLEM - EXPOSED HOT WIRES FROM DAMAGED POWER ENTRY MODULE SHORTED OUT BED'S POWER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAD NO POWER. IT IS UNK IF THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IN TOUCH ZU AC POWERED HOSPITAL BED FNL STRYKER MEDICAL 2141 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK