FDA Adverse Event Malfunction Summary report: N

IN TOUCH ZU

MDR report key: 2091216 · Received April 20, 2011

Report

Report Number
1831750-2011-03810
Event Type
Malfunction
Date Received
April 20, 2011
Date of Event
September 27, 2010
Report Date
September 27, 2010
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END WON'T LOWER ALL THE WAY DOWN. NO ADVERSE CONSEQUENCES HAVE BEEN 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