NeoConnect Enteral Extension Set PEXT-60YNCRecalls & reported problems
Neomed, Inc. · 60" Bifurcated Enteral Extension Set with ENFit Connector, Purple · Class 2
All models of NeoConnect Enteral Extension Set (4)
Data updated Oct 16, 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 00817584012042), received between Feb 12, 2020 and Feb 12, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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 16, 2026.
Most reported problems
Device problems
- Fluid/Blood Leak1
- Leak/Splash1
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 12, 2020Fluid/Blood Leak
TUBING LEAKING DURING INFANT FEEDING AT THE UNION OF TUBING AND MALE HUB. RECURRING PROBLEM WITH THIS PRODUCT AT THIS FACILITY FOR APPROXIMATELY 5 MONTHS. THE MANUFACTURER HAS BEEN NOTIFIED AND PRODUCT HAS BEEN RETURNED; THE MANUFACTURER SAYS THEY ARE INVESTIGATING. THE PROBLEM CONTINUES TO OCCUR. THERE ARE MULTIPLE REPORTS FOR THIS ISSUE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9699589 ↗MalfunctionFeb 12, 2020Leak/Splash
LEAKING BETWEEN CONNECTION FROM OROGASTRIC TUBE AND EXTENSION TUBING, AT THE FEMALE HUB. RECURRING PROBLEM WITH THIS PRODUCT AT THIS FACILITY FOR APPROXIMATELY 5 MONTHS. THE MANUFACTURER HAS BEEN NOTIFIED AND PRODUCT HAS BEEN RETURNED; THE MANUFACTURER SAYS THEY ARE INVESTIGATING. THE PROBLEM CONTINUES TO OCCUR. THERE ARE MULTIPLE REPORTS FOR THIS ISSUE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9699231 ↗
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-05055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-06055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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