FDA Device Intelligence
Home › MEDIVATORS INC. › Endogator Hybrid Irrigation Tubing

Endogator Hybrid Irrigation Tubing

MEDIVATORS INC. · Model 4000838 · UDI-DI 40677964011212

OCX Prescription
1
510(k) clearances
277
Adverse events
18
Recalls
97
Facilities

Description

ENDOGATOR Hybrid Irrigation Tubing with CO2 Connection for certain Olympus GI Endoscopes and Boston Scientific Endostat II Pump Irrigation units.

Recalls

DateFirmReason
2026-03-31Erbe Medical, LLCDevices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water fl
2026-03-31Erbe Medical, LLCDevices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water fl
2022-07-29Hobbs Medical, Inc.Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration
2022-07-29Hobbs Medical, Inc.Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.