FDA Adverse Event Malfunction Summary report: N

CHARGER

MDR report key: 2243492 · Received August 19, 2011

Report

Report Number
8030916-2011-00055
Event Type
Malfunction
Date Received
August 19, 2011
Date of Event
July 25, 2011
Report Date
July 25, 2000
Manufacturer
LIKO AB
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CUSTOMER WAS ADVISED TO REMOVE THE CHARGER FROM SERVICE AND THEY COMPLETED. REPLACEMENT CHARGER WAS PROVIDED TO CUSTOMER. LIFT IS BACK IN SERVICE.

Description of Event or Problem · 1

CUSTOMER ALLEGED THAT WIRES WERE COMING OUT OF THE CHARGER FOR THE LIFT AND WERE SPLICED. CHARGER WAS SPARKING. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CHARGER ACCESSORY FSA LIKO AB

Patients

Seq Age Sex Outcome Treatment
1