NeoConnect Enteral Feeding Tube PFTL6.5P-NCRecalls & reported problems
Neomed, Inc. · PUR Enteral Feeding Tube with ENFit Connector, Purple 6.5Fr X 90cm · Class 2
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 00817584011755), received between Apr 6, 2020 and Apr 6, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (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.
Most reported problems
Device problems
- Leak/Splash1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2020Leak/Splash
BEGAN LEAKING AT JUNCTION WHERE TUBING MEETS PURPLE HUB. FEEDING TUBE HAD TO BE CHANGED OUT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9928224 ↗
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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