FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 2880845 · Received December 20, 2012

Report

Report Number
1525712-2012-03166
Event Type
Malfunction
Date Received
December 20, 2012
Report Date
December 19, 2012
Manufacturer
INVACARE TAYLOR STREET
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). THE DEALER REPORTED THAT THE RPA600-1 PATIENT LIFT HAD TO BE RAISED TO THE HIGHEST POSITION PRIOR TO DESCEND. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE TAYLOR STREET RPA600-1

Patients

Seq Age Sex Outcome Treatment
1 Other