FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3191563 · Received June 26, 2013

Report

Report Number
9616091-2013-01078
Event Type
Malfunction
Date Received
June 26, 2013
Date of Event
May 28, 2013
Report Date
May 31, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

END USER ALLEGES THE LEFT FRONT RIGGING BROKE AND LEFT SIDE CLOTHING GUARD HAVE BOTH BROKEN IN THE LAST WEEK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
290351 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4

Patients

Seq Age Sex Outcome Treatment
1 59 Other