FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3191422 · Received June 26, 2013

Report

Report Number
1525712-2013-05017
Event Type
Malfunction
Date Received
June 26, 2013
Report Date
May 30, 2013
Manufacturer
UNKNOWN
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

PROVIDER STATES UPHOLSTERY IS COMING APART.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
291269 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other