FDA Adverse Event Summary report: N

TOLLOS IQ TECHNOLOGY LIFT SERIES

MDR report key: 3420116 · Received October 11, 2013

Report

Report Number
3420116
Date Received
October 11, 2013
Date of Event
October 7, 2013
Report Date
October 11, 2013
Manufacturer
TOLLOS, INC.
Product Code
FNG
Report Source
User Facility report
Reporter Location
DE, US

Narratives

Description of Event or Problem · 1

THE CEILING LIFT IN ICU FELL FROM THE CEILING. I PRESSED THE DOWN BUTTON TWICE ON THE REMOTE BUT IT SOUNDED LIKE THE MOTOR WAS JAMMED. I PRESSED THE DOWN BUTTON A THIRD TIME AND THE LIFT RELEASED FROM THE BELT AND RAPIDLY SLAMMED DOWN FROM THE CEILING. THE LIFT WAS NOT POSITIONED OVER THE PATIENT, SO NO HARM CAME TO THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
522548 TOLLOS IQ TECHNOLOGY LIFT SERIES LIFT, PATIENT, AC-POWERED FNG TOLLOS, INC. CIRRUS 600 *

Patients

Seq Age Sex Outcome Treatment
1 *