FDA Adverse Event Malfunction Summary report: N

IN TOUCH ZU

MDR report key: 2210217 · Received July 11, 2011

Report

Report Number
1831750-2011-06893
Event Type
Malfunction
Date Received
July 11, 2011
Date of Event
June 13, 2011
Report Date
June 13, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

POWER INLET FILTER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE CORD SPARKED WHEN PLUGGED IN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 UNK