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Recall database

Olympus Corporation of the Americas recalls

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

Showing 61–72 of 163 recalls

Class IIOngoingZ-1378-2026

Olympus Corporation Of The Americas recalls Olympus Thunderbeat

Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of…PAFeb 25, 2026

Class IIOngoingZ-1377-2026

Olympus Corporation Of The Americas recalls Olympus Thunderbeat

Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of…PAFeb 25, 2026

Class IIOngoingZ-1376-2026

Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm

Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of…PAFeb 25, 2026

Class IIOngoingZ-1375-2026

Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm

Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of…PAFeb 25, 2026

Class IIOngoingZ-1374-2026

Olympus Corporation Of The Americas recalls Olympus Thunderbeat

Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of…PAFeb 25, 2026

Class IIOngoingZ-1373-2026

Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm

Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of…PAFeb 25, 2026

Class IIOngoingZ-1372-2026

Olympus Corporation Of The Americas recalls Olympus Thunderbeat

Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of…PAFeb 25, 2026

Class IIOngoingZ-1371-2026

Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm

Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of…PAFeb 25, 2026

Class IOngoingZ-1354-2026

Olympus Corporation Of The Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of…

Issue with software algorithm which may lead to overpressure events.

Olympus Corporation of…PAFeb 25, 2026

Class IOngoingZ-1353-2026

Olympus Corporation Of The Americas recalls Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation of…

Issue with software algorithm which may lead to overpressure events.

Olympus Corporation of…PAFeb 25, 2026

Class IOngoingZ-1352-2026

Olympus Corporation Of The Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of th…

Issue with software algorithm which may lead to overpressure events.

Olympus Corporation of…PAFeb 25, 2026

Class IIOngoingZ-1297-2026

Olympus Corporation Of The Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog N…

Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of…PAFeb 11, 2026