FDA Adverse Event Summary report: N

SUCTION APPARATUS, PATIENT CARE

MDR report key: 3903144 · Received June 30, 2014

Report

Report Number
1531186-2014-02282
Date Received
June 30, 2014
Report Date
May 28, 2014
Manufacturer
EMG TECHNOLOGY CO. LTD
Product Code
DWM
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
RI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER SUCTION IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
380480 SUCTION APPARATUS, PATIENT CARE 870.5050 DWM EMG TECHNOLOGY CO. LTD IRC1135

Patients

Seq Age Sex Outcome Treatment
1 Other