← All recalls
FDAFood & Allergies2025-12-18
Single use ligating device
Product
Single use ligating device
Reason for recall
PolyLoop device may fail to detach as expected and become anchored to patient anatomy
Company
Olympus Corporation
More recalls for Olympus
FDAFood & Allergies2026-01-16
Olympus
ViziShot 2 FLEX (19G) EBUS -TBNA needles
Device & Drug Safety - Defect
See details →
FDAFood & Allergies2025-11-03
Olympus
Bronchofiberscopes and bronchovideoscopes
Potential for endobronchial combustion
See details →
FDAFood & Allergies2025-09-22
Olympus
ViziShot 2 FLEX (19G) EBUS -TBNA needles
Device Components May Detach During Procedures
See details →
