NeoConnect Enteral Feeding Tube PFTL5.0P-NCRecalls & reported problems
Neomed, Inc. · PUR Enteral Feeding Tube with ENFit Connector, Purple 5Fr X 90cm · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00817584011748), received between Apr 6, 2020 and Oct 20, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Migration or Expulsion of Device” (2 reports).
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.
Most reported problems
Device problems
- Migration or Expulsion of Device2
- Detachment of Device or Device Component1
Patient problems
- No Consequences Or Impact To Patient1
- Pressure Sore/Ulcer1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 20, 2020Migration or Expulsion of Device; Migration or Expulsion of Device
IT WAS REPORTED THAT THE NASOGASTRIC (NG) TUBE KEPT MIGRATING OUT OF THE PATIENT. DURING THE FIRST MIGRATION INCIDENT, AT 7:28PM, THE INFANT PATIENT WAS BEARING DOWN AND THE NG TUBE WAS "BOWING OUT" ABOUT 3CM. THE TUBE WAS PUT BACK INTO PLACE. LATER AT 8PM THE INFANT WAS FOUND TO BE PULLING ON THE TUBE. THE TUBE WAS PUT BACK IN PLACE AND RE-TAPED WITH EXUDERM AND ENDOTRACHEAL TUBE TAPE, WHICH HAD BEEN USED TWICE FOR RE-TAPING DURING THE DAY SHIFT. THEN LATER AGAIN AT 10:53PM THE INFANT SNEEZED AND THE NG TUBE CAME ALMOST ALL OF THE WAY OUT. THE INFANT WAS SWADDLED, AND COULD NOT PULL ON THE TUBE WITH THEIR HANDS. NEW TAPE WAS USED TO SECURE THE NG TUBE. AT 11:07PM THE INFANT SNEEZED AGAIN AND THE NG TUBE CAME ALMOST ALL THE WAY OUT. AGAIN THE NG TUBE WAS PUT BACK IN PLACE, THIS TIME WITH THE ADDITION OF TEGADERM AS AN ADDITIONAL SECUREMENT. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10707783 ↗MalfunctionApr 6, 2020Migration or Expulsion of Device; Detachment of Device or Device Component
NG TUBE FOR INFANT WITH SCREW IN END-PIECE. WITH THIS DEVICE THE CAP IS SECURED TO THE FEEDING TUBE BY ITS LOOP BUT CAN FREELY MIGRATE UP AND DOWN LENGTH OF TUBE WHEN OPENED FOR PERIOD OF TIME IN WHICH FEEDING IS ADMINISTERED BY FEEDING PUMP. INFANT WAS NOTED TO HAVE MOVED HIS HEAD DURING FEEDING AND SCREW CAP MIGRATED DOWN LENGTH OF TUBE AND PUT PRESSURE ON INFANT'S FACE. SMALL INDENTATION NOTED ON FACE AT END OF FEEDING WHEN SYRINGE WAS DETACHED AND RN SOUGHT SCREW CAP END TO CLOSE OFF END OF FEEDING TUBE. CONCERN OVER PRESSURE ULCER POTENTIAL OR CHOKING HAZARD DUE TO FREELY MOVABLE PIECE.
Patient problems: Pressure Sore/Ulcer
MAUDE report 9928225 ↗
Other Tube, Nasogastric devices
- Bard® Nasogastric Sump Tube with Enfit™ EN0042140C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall4 reports
- Bard® Nasogastric Sump Tube with Enfit™ EN0042120C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall2 reports
- Bard® Nasogastric Sump Tube with Enfit™ EN0042160C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall2 reports
- Bard® Nasogastric Sump Tube with Enfit™ EN0042180C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall2 reports
- Bard® Nasogastric Sump Tube with Enfit™ EN0042100C. R. Bard, Inc. · TUBE, NASOGASTRIC1 recall0 reports
- Bard® Nasogastric Sump Tube 0042160C. R. Bard, Inc. · TUBE, NASOGASTRIC13 reports
- ENFit PU Feeding Tube PFTM5.0P-NCAvanos Medical, Inc. · TUBE, NASOGASTRIC10 reports
- ENFit PU Feeding Tube PFTL6.5P-NCAvanos Medical, Inc. · TUBE, NASOGASTRIC8 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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