FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3932481 · Received July 14, 2014

Report

Report Number
1525712-2014-03638
Event Type
Malfunction
Date Received
July 14, 2014
Report Date
June 9, 2014
Manufacturer
UNKNOWN
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE RPA450-1 LIFT ACTUATOR IS NOISY AND STARTING TO NOT HOLD. CUSTOMER STATES ON OCCASION IT STARTS TO COME BACK DOWN BUT IT'S NOT ALL THE TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
410883 NON AC-POWERED PATIENT LIFT 880.5510 FSA UNKNOWN RPA450-1

Patients

Seq Age Sex Outcome Treatment
1 Other