FDA Adverse Event Malfunction Summary report: N

VOYAGER

MDR report key: 1070444 · Received July 3, 2008

Report

Report Number
9681684-2008-00014
Event Type
Malfunction
Date Received
July 3, 2008
Date of Event
June 12, 2008
Report Date
July 3, 2008
Manufacturer
BHM MEDICAL, INC.
Product Code
FNG
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE FACILITY REPORTS DURING TRANSFER FROM THE RECLINER CHAIR TO THE BED, THE POST AT THE FOOT END OF THE BED CAME LOOSE AND FELL DOWN. THE LIFT HIT THE RESIDENT ON THE HEAD. THE RESIDENT WAS EIGHT INCHES OFF THE BED. NO INJURIES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VOYAGER CEILING LIFT FNG BHM MEDICAL, INC.

Patients

Seq Age Sex Outcome Treatment
1