FDA Adverse Event Summary report: N

AMS-372 60" ENTERAL FEEDING SET

MDR report key: 1935571 · Received November 23, 2010

Report

Report Number
1935571
Date Received
November 23, 2010
Date of Event
October 29, 2010
Report Date
November 23, 2010
Manufacturer
CHURCHILL MEDICAL SYSTEMS, INC.
Product Code
KNT
Report Source
User Facility report
Reporter Location
MD, US

Narratives

Description of Event or Problem · 1

PATIENT'S FEEDING TUBE WAS CONNECTED TO THE PERIPHERAL IV INSTEAD OF THE GAVAGE TUBE. THIS WAS A MEDICAL MISCONNECTION: THE ENTERAL FEEING TUBE WAS COMPATIBLE WITH LUER-LOCK/PIV CONNECTOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AMS-372 60" ENTERAL FEEDING SET ENTERAL FEEDING SET KNT CHURCHILL MEDICAL SYSTEMS, INC. AMS-372 1006013

Patients

Seq Age Sex Outcome Treatment
1 3 DA