FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 2930925 · Received January 28, 2013

Report

Report Number
1531186-2013-00317
Date Received
January 28, 2013
Report Date
January 26, 2013
Manufacturer
JUMAO MEDICAL EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

MDR DECISION DATE: (B)(6). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PER DEALER THE RUBBER CAME OFF OF THE REAR WHEEL. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
36668 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V20RLR

Patients

Seq Age Sex Outcome Treatment
1 Other