FDA Adverse Event Other Summary report: N

LIKO VIKING L UNIVERSAL SLING BAR ON PATIENT LIFT

MDR report key: 746205 · Received July 5, 2006

Report

Report Number
MW1039584
Event Type
Other
Date Received
July 5, 2006
Date of Event
June 25, 2006
Report Date
June 27, 2006
Manufacturer
LIKO
Product Code
FSA
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
ME, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

UNIVERSAL SLING BAR 450 ALUMINUM BECAME DETACHED ON VIKING L LIFT MANUFACTURED BY LIKO. THIS OCCURRED WHILE PT BEING TRANSFERRED. PT FELL ONTO BED WITHOUT SUSTAINING INJURY. WHEN CO NOTIFIED THEY FAXED A COPY OF URGENT MEDICAL DEVICE RECALL DATED 06/19/06 WHICH WE HAD NOT REC'D.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIKO VIKING L UNIVERSAL SLING BAR ON PATIENT LIFT PATIENT LIFT FSA LIKO * *

Patients

Seq Age Sex Outcome Treatment
1 49 YR Other