FDA Adverse Event Malfunction Summary report: N

IN TOUCH ZU

MDR report key: 2072527 · Received April 19, 2011

Report

Report Number
1831750-2011-03776
Event Type
Malfunction
Date Received
April 19, 2011
Date of Event
September 15, 2010
Report Date
September 15, 2010
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

RESULT: BREAKER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THERE WAS NO POWER TO AUXILIARY OUTLETS. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1