FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2983083 · Received February 28, 2013

Report

Report Number
1531186-2013-00769
Date Received
February 28, 2013
Report Date
February 26, 2013
Manufacturer
CONSMA
Product Code
ITJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

MDR DECISION DATE: (B)(6). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PROVIDER STATES THE LEG SNAPPED. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
86102 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ CONSMA 65650

Patients

Seq Age Sex Outcome Treatment
1 Other