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Olympus Corporation of the Americas Recalls
414 recalls on record · October 7, 2015 to July 29, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and treatment in urological applicatio
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;
Hazard: Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 10 cm, Inline Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 35 cm, Inline Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 45 cm Inline Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5mm, 35 cm, Pistol Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 45 cm, Pistol Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 35 cm, Front-Actuated Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 45 cm Front-Actuated Grip
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 35 cm, Front-Actuated Grip Type S
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S
Hazard: Firm is initiating a removal due to continued reports of adverse events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of the abdominal cavity, and automat
Hazard: Issue with software algorithm which may lead to overpressure events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation of the abdominal cavity, and automa
Hazard: Issue with software algorithm which may lead to overpressure events.
February 25, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic
Hazard: Issue with software algorithm which may lead to overpressure events.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0725; Software
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025 Product Description: These instr
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020 Product Description: These instr
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0725 Product Description: These ins
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3030 Product Description: These instr
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1530 Product Description: These instr
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These instr
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0730 Product Description: These ins
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0720 Product Description: These ins
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These ins
Hazard: Devices which did not undergo thermoforming could deform and lose performance.
February 11, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-411Q-0730 Product Description: These ins
Hazard: Devices which did not undergo thermoforming could deform and lose performance.