FDA Adverse Event Malfunction Summary report: N

IV FLOW CONTROL EXTENSION SET WITH SMART SITE

MDR report key: 505135 · Received December 18, 2003

Report

Report Number
MW1030634
Event Type
Malfunction
Date Received
December 18, 2003
Manufacturer
LIV MEDICAL PRODUCTS, MEDIC ACS
Product Code
FPA
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
KY, US
Reporter Occupation
NURSE

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IV FLOW CONTROL EXTENSION SET WITH SMART SITE RATE CONTROL DEVICE FPA LIV MEDICAL PRODUCTS, MEDIC ACS RF-1001-1 303079

Patients

Seq Age Sex Outcome Treatment
1 *