Olympus Corporation of the Americas recalls

176 recalls on record · latest: March 25, 2026

Official U.S. recall history for Olympus Corporation of the Americas, compiled from official government records.

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Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus OER-…

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.

March 25, 2026 · Medical device recalls Moderate risk XXX

Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 25cm. Model Number: TB2-0525FC.

March 23, 2026 · Medical device recalls Moderate risk Potential for detachment of a distal tip component of the device during use.

Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 35cm. Model Number: TB2-0535FC.

March 23, 2026 · Medical device recalls Moderate risk Potential for detachment of a distal tip component of the device during use.

Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.

March 23, 2026 · Medical device recalls Moderate risk Potential for detachment of a distal tip component of the device during use.

Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 45cm. Model Number: TB2-0545FC.

March 23, 2026 · Medical device recalls Moderate risk Potential for detachment of a distal tip component of the device during use.

Olympus Corporation of the Americas recalls Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog N…

February 27, 2026 · Medical device recalls Moderate risk Following a complaint investigation, Olympus identified a potential defect in t…

Olympus Corporation of the Americas recalls Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/C…

February 27, 2026 · Medical device recalls Moderate risk Following a complaint investigation, Olympus identified a potential defect in t…

Olympus Corporation of the Americas recalls Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm Product Name: HALO PKS Cutting Forceps Model/Catalog Number: HAC…

February 25, 2026 · Medical device recalls Moderate risk Olympus identified that the Cutting Forceps contain components for which the su…

Olympus Corporation of the Americas recalls Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Prod…

February 25, 2026 · Medical device recalls Moderate risk Olympus identified that the Cutting Forceps contain components for which the su…

Olympus Corporation of the Americas recalls Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar Cutting Forceps Mod…

February 25, 2026 · Medical device recalls Moderate risk Olympus identified that the Cutting Forceps contain components for which the su…

Olympus Corporation of the Americas recalls Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Cat…

February 25, 2026 · Medical device recalls Moderate risk Olympus identified that the Cutting Forceps contain components for which the su…

Olympus Corporation of the Americas recalls Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Produ…

February 25, 2026 · Medical device recalls Moderate risk Olympus identified that the Cutting Forceps contain components for which the su…

Olympus Corporation of the Americas recalls Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920000…

February 25, 2026 · Medical device recalls Moderate risk Olympus identified that the Cutting Forceps contain components for which the su…

Olympus Corporation of the Americas recalls Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 3005PK Produc…

February 25, 2026 · Medical device recalls Moderate risk Olympus identified that the Cutting Forceps contain components for which the su…

Olympus Corporation of the Americas recalls Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.

February 12, 2026 · Medical device recalls Moderate risk The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pr…

Olympus Corporation of the Americas recalls Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.

February 12, 2026 · Medical device recalls Moderate risk The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pr…

Olympus Corporation of the Americas recalls Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.

February 12, 2026 · Medical device recalls Moderate risk The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pr…

Olympus Corporation of the Americas recalls Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.

February 12, 2026 · Medical device recalls Moderate risk The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pr…

Olympus Corporation of the Americas recalls Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be…

January 29, 2026 · Medical device recalls Moderate risk Potential for rubber fragment detachment during use.

Olympus Corporation of the Americas recalls Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be a…

January 29, 2026 · Medical device recalls Moderate risk Potential for rubber fragment detachment during use.

Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic su…

January 16, 2026 · Medical device recalls High risk Issue with software algorithm which may lead to overpressure events.

Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation of the abdominal cavity, and automatic…

January 16, 2026 · Medical device recalls High risk Issue with software algorithm which may lead to overpressure events.

Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of the abdominal cavity, and automatic…

January 16, 2026 · Medical device recalls High risk Issue with software algorithm which may lead to overpressure events.

Olympus Corporation of the Americas recalls Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lithotripsy System - Re…

January 8, 2026 · Medical device recalls Moderate risk Mis-wired component-the improperly wired component can result in additional noi…

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC433Q-0720; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0720; Software Version: N/A Product De…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0725 Product Description: These inst…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1530 Product Description: These instru…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC431Q-0720 Product Description…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC412Q-0215; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog N…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0330; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0730; Software Version: N/A Product De…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020 Product Description: These instru…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3030 Product Description: These instru…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0730; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0320; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0730; Software Version: N/A Product De…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number:KD-VC433Q-0730; Software Ve…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Brand Name: CleverCut Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0320; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-411Q-0720 Product Description: These inst…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC431Q-0730; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0720; Software Version: N/A Product De…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0720; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-411Q-0730 Product Description: These inst…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0725; Software V…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0720 Product Description: These inst…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-431Q-0720 Product Description: These inst…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025 Product Description: These instru…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0730 Product Description: These inst…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0725; Software Version: N/A Product De…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0330; Software Version: N/A Product De…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These inst…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These instru…

January 7, 2026 · Medical device recalls Moderate risk Devices which did not undergo thermoforming could deform and lose performance.

Olympus Corporation of the Americas recalls Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes M…

November 14, 2025 · Medical device recalls Moderate risk Ongoing investigations identified additional instances of the device Generator…

Olympus Corporation of the Americas recalls Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Mo…

November 14, 2025 · Medical device recalls Moderate risk Ongoing investigations identified additional instances of the device Generator…

Olympus Corporation of the Americas recalls Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Generator Model/Catalog N…

November 14, 2025 · Medical device recalls Moderate risk Ongoing investigations identified additional instances of the device Generator…

Olympus Corporation of the Americas recalls Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and treatment in urological applicati…

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic applicatio…

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applicatio…

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for urologic applicati…

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological applications.

November 11, 2025 · Medical device recalls Moderate risk Complaints of the ceramic tip of the resection sheath breaking have been receiv…

Olympus Corporation of the Americas recalls Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog Number: HX-400U-30 Used with an O…

October 30, 2025 · Medical device recalls High risk Potential that the ligation loop was unable to release or detach as expected du…

Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 45 cm Inline Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 35 cm, Inline Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 45 cm Front-Actuated Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 35 cm, Front-Actuated Grip Type S

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 10 cm, Inline Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 45 cm, Pistol Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 35 cm, Front-Actuated Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.

Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5mm, 35 cm, Pistol Grip

October 22, 2025 · Medical device recalls Moderate risk Firm is initiating a removal due to continued reports of adverse events.