FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3000582 · Received March 12, 2013

Report

Report Number
3004493922-2013-00582
Event Type
Malfunction
Date Received
March 12, 2013
Report Date
February 26, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

(B)(4) HAS BEEN INITIATED FOR THIS ISSUE. THE MALFUNCTION HAS NOT BEEN CONFIRMED.

Description of Event or Problem · 1

PROVIDER STATES PUMP IS NOT HOLDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
102898 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9098P

Patients

Seq Age Sex Outcome Treatment
1 Other