FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4094056 · Received September 16, 2014

Report

Report Number
9616091-2014-01886
Event Type
Malfunction
Date Received
September 16, 2014
Report Date
August 22, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES TWO SPOKES ON LEFT WHEEL WERE CRACKED IN HALF OUT OF BOX. RECEIVED (B)(6)2014.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
570888 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TRSX50FBP

Patients

Seq Age Sex Outcome Treatment
1 Other