FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3243576 · Received July 23, 2013

Report

Report Number
3004493922-2013-01597
Event Type
Malfunction
Date Received
July 23, 2013
Report Date
July 2, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THE RHL450-1 HYDRAULIC LIFT HAS SEIZED UP, CAUSING THE HANDLE TO BREAK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
344403 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU RHL450-1

Patients

Seq Age Sex Outcome Treatment
1 Other