FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 2960083 · Received February 13, 2013

Report

Report Number
1525712-2013-01110
Event Type
Malfunction
Date Received
February 13, 2013
Report Date
February 13, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(6) -THE DEALER REPORTED THAT THE 9099P PATIENT TRANSPORT HYDRAULIC LIFT WAS LEAKING OIL AND WOULD NOT HOLD WEIGHT. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
62357 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9099P

Patients

Seq Age Sex Outcome Treatment
1 Other