FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3191560 · Received June 26, 2013

Report

Report Number
9616091-2013-01076
Event Type
Malfunction
Date Received
June 26, 2013
Report Date
June 3, 2013
Manufacturer
INVAMEX
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER (B)(6), LEGS ON THE LIFT WILL NOT REMAIN IN THE LOCKED POSITION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
290350 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVAMEX RPL450-1

Patients

Seq Age Sex Outcome Treatment
1 Other