FDA Adverse Event Malfunction Summary report: N

IN TOUCH ZU

MDR report key: 2141401 · Received June 1, 2011

Report

Report Number
1831750-2011-05370
Event Type
Malfunction
Date Received
June 1, 2011
Date of Event
May 5, 2011
Report Date
May 5, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

BREAKER TRIPPED IN AUXILIARY OUTLET.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE XPRT MATTRESS WAS NOT DETECTED. THE FOOT AUXILIARY OUTLET HAD IT'S BREAKER TRIPPED. 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