FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3051663 · Received April 10, 2013

Report

Report Number
3004493922-2013-00785
Event Type
Malfunction
Date Received
April 10, 2013
Report Date
March 14, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

CONSUMER ALLEGES THAT THE LIFT WILL NOT STAY RAISED, STATED IT WILL LOWER WITH OR WITHOUT WEIGHT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
152279 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805P

Patients

Seq Age Sex Outcome Treatment
1 Other