FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3233130 · Received July 18, 2013

Report

Report Number
1531186-2013-03224
Date Received
July 18, 2013
Report Date
June 26, 2013
Manufacturer
LERADO GLOBAL
Product Code
ILS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES FRONT PLASTIC CLAMP SNAPPED AT BOLT ATTACHMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
333552 DAILY ACTIVITY ASSIST DEVICES 890.5050 ILS LERADO GLOBAL 1302RTS

Patients

Seq Age Sex Outcome Treatment
1 Other