FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3022203 · Received March 26, 2013

Report

Report Number
3004493922-2013-00678
Event Type
Malfunction
Date Received
March 26, 2013
Report Date
February 28, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

CALLER STATES HER HUSBAND WAS DISCHARGED FROM VA WITH A STANDING RPS350-1 LIFT AND A STANDING SLING. CALLER STATES SLING IS NOT SAFE AND IS FRAYING AT THE END. SAYS IT IS NOT STABLE FOR HER HUSBAND.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
124653 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU RPS350-1

Patients

Seq Age Sex Outcome Treatment
1 Other