FDA Adverse Event Other Summary report: N

IN TOUCH ZU

MDR report key: 2326706 · Received October 20, 2011

Report

Report Number
1831750-2011-11042
Event Type
Other
Date Received
October 20, 2011
Date of Event
September 22, 2011
Report Date
September 22, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

TRIPPED AUXILIARY POWER BREAKER DUE TO ANOMALY IN ELECTRICAL CIRCUIT.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE THERE WAS A LOSS OF POWER TO THE AUXILIARY OUTLET OF THE BED. NO PATIENT 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