FDA Device Intelligence
HomeUS Endoscopy › Torrent

Torrent

US Endoscopy · Model 00711563 · UDI-DI 00816765011645

OCX Prescription
10
510(k) clearances
261
Adverse events
18
Recalls
98
Facilities

Description

The Torrent irrigation tubing is intended to provide irrigation via irrigation fluids, such as sterile water, during gastrointestinal endoscopic procedures when used in conjunction with an irrigation pump or electrosurgical unit.

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.