Halyard 47206Recalls & reported problems

Avanos Medical, Inc. · CORTRAK 2 Enteral Access System-Refurbished · Class 2

Adverse event reports: 0
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

Mar 21, 2022Terminated
Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately. CONFIRM placement of the NG/NI tube per institution protocol.
Z-1032-2022 · Root cause: Device Design · FDA record ↗

Device details

UDI-DI	`10680651472066`
Brand	Halyard
Model	47206
Catalog no.	P20-0950
Company	Avanos Medical, Inc.
Product code	KNT · TUBES, GASTROINTESTINAL (AND ACCESSORIES)
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Nov 16, 2018

Device type (GMDN): Enteral tube tracking system

A mains electricity (AC-powered) portable electronic device assembly, typically with rechargeable battery, designed to detect, record, and display an electromagnetic (EM) signal emitted from a transmitter in an enteral feeding tube stylet to facilitate the placement of the enteral tube, by providing a graphic display representing the path of the tube tip. It consists of an electromagnetic receiver placed on the epigastrium, a visual display/control unit which displays real-time anterior and cross-sectional representational views of the transmitter location and track, and a separately supplied single-use enteral feeding tube stylet which incorporates an electromagnetic transmitter in the tip.

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

Bard® DigniShield® Stool Management System SMS002
C. R. Bard, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)
2 deaths525 reports
CORTRAK* 2 ENTERAL ACCESS SYSTEM 20-0950
Avanos Medical, Inc. · Tubes, gastrointestinal (and accessories)
1 recall22 deaths134 reports
Bard Tri-Funnel Replacement Gastrostomy Tube 000720
Bard Access Systems, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)
1 death170 reports
EndoVive Safety PEG Kit M00566470
Boston Scientific Corporation · TUBES, GASTROINTESTINAL (AND ACCESSORIES)
1 recall1 death111 reports
Kangaroo 8884711253
Cardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)
152 reports
Kangaroo 8884711253E
Cardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)
100 reports
NutraGlide Nasal Feeding Tube ENFT-05055-I
Applied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)
2 recalls0 reports
NutraGlide Nasal Feeding Tube ENFT-06090-I
Applied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)
2 recalls0 reports

All TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.