Recall database

Ligator, Esophageal recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–1 of 1 recalls

Class IOngoingZ-0570-2026

Olympus Corporation Of The Americas recalls Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog…

Potential that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally fixed around patient anatomy.

Esophageal Ligator
Process control

Olympus Corporation of…PADec 3, 2025