FDA Device Intelligence
Home › US Endoscopy › Lariat

Lariat

US Endoscopy · Model 00711097 · UDI-DI 00816765015247

FDI Prescription
1
510(k) clearances
4,640
Adverse events (10 deaths)
18
Recalls
60
Facilities

Description

The Lariat snare is an electrosurgical device designed to be used to endoscopically grasp, dissect, and transect tissue during Gastrointestinal (GI) endoscopic procedures.

Recalls

DateFirmReason
2025-10-06Olympus Corporation of the AmericasSterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.
2025-10-06Olympus Corporation of the AmericasSterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.
2021-01-19Boston Scientific CorporationPackaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.
2021-01-19Boston Scientific CorporationPackaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.
2021-01-19Boston Scientific CorporationPackaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.
2020-07-06Boston Scientific CorporationBSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended would be a prolonged pr
2020-07-06Boston Scientific CorporationBSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended would be a prolonged pr
2020-07-06Boston Scientific CorporationBSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended would be a prolonged pr
2020-07-06Boston Scientific CorporationBSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended would be a prolonged pr
2020-07-06Boston Scientific CorporationBSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended would be a prolonged pr

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.