Cortrak 2 Enternal access device 46051Recalls & reported problems
Avanos Medical, Inc. · CORTRAK* 2 Nasogastric/Nasointestinal Feeding Tube with Electromagnetic Transmitting Stylet with ENFit® Connector · Class 2
All models of Cortrak 2 Enternal access device (14)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00350770460512), received between Feb 17, 2026 and Feb 17, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 17, 2026Break
FDA MAUDE ADVERSE EVENT REPORT MDR REPORT KEY 21813548, "NURSE REPORTED THAT PATIENT COULD TASTE HIS MEDICATIONS THIS AM [MORNING], WHICH WERE ADMINISTERED VIA SMALL BORE NGT [NASOGASTRIC TUBE]. REPEAT CXR [CHEST X-RAY] CONFIRMED TUBE PLACEMENT. RD [REGISTERED DIETITIAN] NOTED COIL ON X-RAY AND CONCERN FOR COMPROMISED INTEGRITY OF TUBE. RD PULLED OLD TUBE, AND IT WAS BROKEN AT THE 64CM MARK WITH NOTED BALLOONING AT BROKEN PART. GI [GASTROINTESTINAL] WAS CONSULTED, XR [X-RAYS] WERE ORDERED, PT (PATIENT) UNDERWENT EGD [ESOPHAGOGASTRODUODENOSCOPY] FOR REMOVAL OF BROKEN PIECE RETAINED IN STOMACH."
Patient problems: Foreign Body In Patient
MAUDE report 24367367 ↗
Other Tubes, gastrointestinal (and accessories) devices
- Bard® DigniShield® Stool Management System SMS002C. R. Bard, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 deaths525 reports
- CORTRAK* 2 ENTERAL ACCESS SYSTEM 20-0950Avanos Medical, Inc. · Tubes, gastrointestinal (and accessories)1 recall22 deaths134 reports
- Bard Tri-Funnel Replacement Gastrostomy Tube 000720Bard Access Systems, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 death170 reports
- EndoVive Safety PEG Kit M00566470Boston Scientific Corporation · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 recall1 death111 reports
- Kangaroo 8884711253Cardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)152 reports
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-05090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- Kangaroo 8884711253ECardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)100 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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