NeoConnect GravityPro PNM-S100NCVRecalls & reported problems
Neomed, Inc. · 100mL GravityPro Enteral Syringe with ENFit Connector, Sterile, Purple · 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 00817584012165), received between Sep 11, 2019 and Sep 11, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Excess Flow or Over-Infusion” (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
- Excess Flow or Over-Infusion1
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.
MalfunctionSep 11, 2019Excess Flow or Over-Infusion
BABY WITH G-TUBE RESTARTING FEEDS VIA GRAVITY/DRIP METHOD. BABY HAS ORDER TO FEED "NEOCATE, 22ML/HR TO GRAVITY." 70ML OF MILK WAS DRAWN UP IN 100ML NEOMED ENFIT SYRINGE, CONNECTED TO AN ABC INFANT ENTERAL FEEDING PUMP, SET TO INFUSE AT 22ML/HR. WHEN RN LOOKED AT SYRING AN HOUR OR SO LATER, THE SYRINGE NO LONGER HAD MILK IN IT, EVEN THOUGH THE PUMP WAS GOING AS EXPECTED AND PLUNGER WAS IN PLACE IN SYRINGE. FEEDING INFUSED TOO QUICKLY, POSSIBLY DUE TO SOME SORT OF "LEAK" IN THE SYSTEM, ALLOWING MILK TO GO IN VIA GRAVITY RATHER THAN THE PRESCRIBED RATE. RN TESTED THE SAME SYRINGE/PUMP WITH WATER AFTER THIS EVENT, AND SAME RESULTS OCCURRED. SYRINGE OF MILK EMPTIED PRIOR TO EXPECTED TIME VIA PUMP. SAME RN TESTED A 2ND 100ML SYRINGE TO SEE IF THE SAME THING WOULD HAPPEN, AND IT INFUSED AS EXPECTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8995174 ↗
Other Enteral Syringes With Enteral Specific Connectors devices
- Cardinal Health 1mlJiangsu Caina Medical Co.,Ltd · Enteral Syringes With Enteral Specific Connectors1 recall5 reports
- Cardinal Health 35mlJiangsu Caina Medical Co.,Ltd · Enteral Syringes With Enteral Specific Connectors1 recall4 reports
- Cardinal Health 60mlJiangsu Caina Medical Co.,Ltd · Enteral Syringes With Enteral Specific Connectors1 recall4 reports
- Cardinal Health 6mlJiangsu Caina Medical Co.,Ltd · Enteral Syringes With Enteral Specific Connectors1 recall0 reports
- Cardinal Health 12mlJiangsu Caina Medical Co.,Ltd · Enteral Syringes With Enteral Specific Connectors1 recall0 reports
- Cardinal Health 3mlJiangsu Caina Medical Co.,Ltd · Enteral Syringes With Enteral Specific Connectors1 recall0 reports
- Medline NON66160Medline Industries, Inc. · Enteral Syringes with enteral specific connectors4 reports
- ENFit Syringe PNM-S60NCAvanos Medical, Inc. · Enteral Syringes with enteral specific connectors3 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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