FDA Adverse Event Other Summary report: N

GOLVO

MDR report key: 1030077 · Received April 3, 2008

Report

Report Number
3006252983-2008-00009
Event Type
Other
Date Received
April 3, 2008
Date of Event
March 3, 2008
Report Date
March 11, 2008
Manufacturer
LIKO AB
Product Code
FSA
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PT WAS BEING TRANSFERRED FROM BED TO WHEELCHAIR USING A GOLVO PT LIFT, SHIFTED WEIGHT AND THE SLING LOOP CAME OFF THE SLING BAR. PT DROPPED AND BROKE TWO RIBS ALSO, CONTUSION TO THE HEAD. IT WAS DISCOVERED THAT THE SAFETY LATCHES WERE MISSING FROM THE SLING BAR USED ON THE GOLVO, AND THAT THE SLING USED IN THE TRANSFER WAS NOT MFG, APPROVED OR DESIGNED FOR USE WITH THIS EQUIPMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GOLVO NON-AC POWERED PT LIFT FSA LIKO AB GOLVO 7007 *

Patients

Seq Age Sex Outcome Treatment
1 92 YR Other