ENDOGATOR hybrid irrigation tubing 100605Recalls & reported problems
Medivators Inc. · Class 2
All models of ENDOGATOR hybrid irrigation tubing (5)
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 00677964060830), received between Dec 14, 2023 and Dec 14, 2023 — 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.
Reports received per month
Most reported problems
Device problems
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 14, 2023Leak/Splash; Leak/Splash
THE USER FACILITY REPORTED THAT THEIR ENDOGATOR HYBRID IRRIGATION TUBING PINCH CLIP UNCLAMPED DURING USE AND CAUSED WATER TO LEAK OUT. NO REPORT OF INJURY OR PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18327146 ↗
Other Endoscopic Irrigation/Suction System devices
- OrcaPod™ SUV-628Boston Scientific Corporation · endoscopic irrigation/suction system79 reports
- Suction Valve EN10232GA Health Company Limited · Endoscopic Irrigation/Suction System1 recall0 reports
- andorate® A/W Channel Cleaning Adapter + 4-piece Valve Kit GAR3846GA Health Company Limited · Endoscopic Irrigation/Suction System1 recall0 reports
- BullDog® 1203-71Diversatek Healthcare, Inc. · Endoscopic Irrigation/Suction System1 recall0 reports
- ERBEFLO CleverCap® 20325-201Erbe Medical, LLC · Endoscopic Irrigation/Suction System1 recall0 reports
- 2-piece valve kit (Suction and Air/Water Valve) EN10229.2GA Health Company Limited · Endoscopic Irrigation/Suction System1 recall0 reports
- 4-piece valve kit(Suction, Air/Water, Biopsy Valves & Auxiliary Water Connector) EN10229.1GA Health Company Limited · Endoscopic Irrigation/Suction System1 recall0 reports
- ERBEFLO CleverCap® 20325-203Erbe Medical, LLC · Endoscopic Irrigation/Suction System1 recall0 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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