FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3250824 · Received July 29, 2013

Report

Report Number
9616091-2013-01331
Event Type
Malfunction
Date Received
July 29, 2013
Report Date
July 10, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

CONSUMER ALLEGES PART NUMBER 1111270 IS BROKEN. DAWN IS A FAMILY FRIEND AND WILL OBTAIN MORE INFORMATION AS TO HOW THIS WAS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
353820 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9SL

Patients

Seq Age Sex Outcome Treatment
1 Other