FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 2863686 · Received December 10, 2012

Report

Report Number
3004493922-2012-00665
Event Type
Malfunction
Date Received
December 10, 2012
Report Date
December 7, 2012
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(6) -THE DEALER REPORTED THAT THE RPL450-2 ROZE PATIENT LIFT INDEX PLATE WAS BROKEN. 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 SUZHOU RPL450-2

Patients

Seq Age Sex Outcome Treatment
1 Other