FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 4040844 · Received August 27, 2014

Report

Report Number
1525712-2014-05094
Event Type
Malfunction
Date Received
August 27, 2014
Report Date
July 30, 2014
Manufacturer
UNKNOWN
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER CAREGIVERS

Narratives

Description of Event or Problem · 1

FACILITY STATES UNIT SEEMS TO HAVE A SHORT IN THE CORD THAT RUNS FROM ACTUATOR TO BATTERY. WILL NOT RAISE NOR LOWER AT TIMES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
519602 NON AC-POWERED PATIENT LIFT 880.5510 FSA UNKNOWN RPL450

Patients

Seq Age Sex Outcome Treatment
1 Other