FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3071951 · Received April 22, 2013

Report

Report Number
1531186-2013-01695
Date Received
April 22, 2013
Report Date
March 27, 2013
Manufacturer
CONSMA
Product Code
BTI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES THE LEFT LEG SNAPPED AT THE WELD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
172252 MECHANICAL WALKER, ROLLATOR 890.3825 BTI CONSMA 65650

Patients

Seq Age Sex Outcome Treatment
1 Other