FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3000603 · Received March 12, 2013

Report

Report Number
3004493922-2013-00584
Event Type
Malfunction
Date Received
March 12, 2013
Report Date
February 14, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PER PROVIDER UNIT WILL INTERMITTENTLY FAIL TO LIFT OR GO DOWN. THE SAME FOR THE LEGS TO OPEN OR CLOSE. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
102937 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU RPS350-2

Patients

Seq Age Sex Outcome Treatment
1 Other