FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 2972606 · Received February 21, 2013

Report

Report Number
9616091-2013-00275
Event Type
Malfunction
Date Received
February 21, 2013
Report Date
February 21, 2013
Manufacturer
INVAMEX
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. CONSUMER ALLEGES THAT THE CROSS BAR UNDERNEATH BROKE AND HE ONLY WEIGHS (B)(6). MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
75618 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TRSX5

Patients

Seq Age Sex Outcome Treatment
1 Other