FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3081714 · Received April 29, 2013

Report

Report Number
1531186-2013-01804
Date Received
April 29, 2013
Report Date
April 3, 2013
Manufacturer
JUMAO MEDICAL EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PER DEALER, THE CUSTOMER IS COMPLAINING THAT THE WHEELS ARE LEAVING BLACK MARKS ON THE FLOOR. HE STATES THE WHEEL LOCK BOLT IS CLOSE THE TIRE WHICH MAY BE CAUSING IT TO RUB, POSSIBLY CAUSING THE TIRE TO RUB OFF. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
185688 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V18RFR

Patients

Seq Age Sex Outcome Treatment
1 Other