Class IIOngoingZ-1489-2026
Olympus Corporation Of The Americas recalls Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. T…
Potential for rubber fragment detachment during use.
Olympus Corporation of…PAMar 11, 2026
Bronchoscope (Flexible Or Rigid) recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–4 of 4 recalls
Class IIOngoingZ-1488-2026
Olympus Corporation Of The Americas recalls Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. Th…
Potential for rubber fragment detachment during use.
Olympus Corporation of…PAMar 11, 2026
Class IIOngoingZ-1383-2026
Auris Health, Inc recalls MONARCH Platform
Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope loading, application will re-initialize to patient-left positi…
Auris Health, IncCAFeb 25, 2026
Class IIOngoingZ-1134-2026
Intuitive Surgical, Inc. recalls Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog N…
Due to probe bags that may have a compromised or incomplete sterile pouch seal.
Intuitive Surgical, In…CAJan 28, 2026