FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3033924 · Received April 3, 2013

Report

Report Number
3004493922-2013-00712
Event Type
Malfunction
Date Received
April 3, 2013
Report Date
March 6, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

THE DEALER REPORTED THAT THE HYDRAULIC LIFT WOULD NOT HOLD WEIGHT AND WOULD GRADUALLY LOWER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
137183 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU GHS350

Patients

Seq Age Sex Outcome Treatment
1 Other