FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3022046 · Received March 26, 2013

Report

Report Number
9616091-2013-00517
Date Received
March 26, 2013
Date of Event
March 6, 2013
Report Date
March 6, 2013
Manufacturer
INVAMEX
Product Code
IOR
Adverse Event
Yes
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 FRAME TWISTED AND SHE FELL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
124494 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T422RDA

Patients

Seq Age Sex Outcome Treatment
1 52 Other