FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3902943 · Received June 30, 2014

Report

Report Number
3008262382-2014-00165
Event Type
Malfunction
Date Received
June 30, 2014
Report Date
May 28, 2014
Manufacturer
INVACARE REHABILITATION EQUIP
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

ACTUATOR NOT HOLDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
379707 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE REHABILITATION EQUIP RPL600-2 LIFT

Patients

Seq Age Sex Outcome Treatment
1 Other