FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 2973221 · Received February 21, 2013

Report

Report Number
1531186-2013-00700
Date Received
February 21, 2013
Date of Event
January 24, 2013
Report Date
February 21, 2013
Manufacturer
JUMAO MEDICAL EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4) - THE DEALER REPORTED THAT THE V18RFR MECHANICAL WHEELCHAIR HAD A BROKEN WHEEL. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
76090 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V18RFR

Patients

Seq Age Sex Outcome Treatment
1 Other