FDA Adverse Event Malfunction Summary report: N

TUBE, FEEDING ENTERAL W/STYLET 5FR 22IN

MDR report key: 1071206 · Received June 15, 2008

Report

Report Number
1071206
Event Type
Malfunction
Date Received
June 15, 2008
Date of Event
May 15, 2008
Report Date
June 15, 2008
Manufacturer
VIASYS HEALTHCARE MEDSYSTEMS
Product Code
FPD
Product Problem
Yes
Report Source
User Facility report
Reporter Location
MI, US

Narratives

Description of Event or Problem · 1

NASOGASTRIC TUBE LEAKING AT THE JOINT WHERE THE HUB MEETS THE TUBE. STILL TOGETHER BUT LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TUBE, FEEDING ENTERAL W/STYLET 5FR 22IN ENTERAL TUBE FPD VIASYS HEALTHCARE MEDSYSTEMS NA NA

Patients

Seq Age Sex Outcome Treatment
1 3 MO