FDA Adverse Event Summary report: N

GH3 LIFT

MDR report key: 3341086 · Received July 29, 2013

Report

Report Number
3341086
Date Received
July 29, 2013
Date of Event
July 20, 2013
Report Date
July 29, 2013
Manufacturer
GULDMANN, INC.
Product Code
FNG
Report Source
User Facility report
Reporter Location
PA, US
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

MOVING PATIENT USING LIFT DEVICE IN ROOM AS LIFT WAS IN DOWN POSITION WOULD NOT MOVE UP. AN ORANGE LIGHT ON THE MACHINE WAS ENGAGE AND THEN THE DEVICE WOULD NOT LIFT THE PATIENT UP. RESET BUTTON WAS PUSHED TO ASSIST BUT DID NOTHING TO CORRECT THE ISSUE. EMERGENCY RELEASE WAS PULLED AND PATIENT WAS SAFELY LOWERED USING MULTIPLE STAFF TO ASSIST.MANUFACTURER RESPONSE FOR PATIENT LIFT, GULDMANN GH3 CEILING LIFT SYSTEM (PER SITE REPORTER).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
354913 GH3 LIFT LIFT, PATIENT, AC-POWERED FNG GULDMANN, INC. GH3 *

Patients

Seq Age Sex Outcome Treatment
1 89 YR