Olympus Corporation of the Americas recalls
84 recalls.
- Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable. - Olympus M3 Gold Autoclavable Lateral Telescope 70. Model Number: M3-70A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the... - Olympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the... - Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. - Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model/Catalog Number: CD-B620LA. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. - Olympus BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector. Model/Catalog Number: CD-B612LA. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. - Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. - Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for the inflation chart label affixed to the shaft of the device to be incorrect and indicate a balloon diameter of 18, 19, or 20 mm, - POWERSEAL 5 MM recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 2, 2026 · Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. - Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 29, 2026 · Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases. - Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 29, 2026 · Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities. - Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Ellik Evacuator Includes Glass Body recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 22, 2026 · Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to... - Olympus Single Use Distal Cover recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 15, 2026 · Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · XXX - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - Olympus Thunderbeat II Shears w/Ultrasonic Mode recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for detachment of a distal tip component of the device during use. - Olympus Thunderbeat II Shears w/Ultrasonic Mode recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for detachment of a distal tip component of the device during use. - Olympus Thunderbeat II Shears w/Ultrasonic Mode recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for detachment of a distal tip component of the device during use. - Olympus Thunderbeat II Shears w/Ultrasonic Mode recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for detachment of a distal tip component of the device during use. - Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the... - Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the... - Brand Name: Olympus PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PKS Cutting Forceps w/Cord recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus HALO PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PK Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus Everest Bipolar Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Mis-wired component-the improperly wired component can result in additional noise on the power supply output. Noise on the ultrasonic input circuit is not... - Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Potential for rubber fragment detachment during use. - Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Potential for rubber fragment detachment during use. - Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3030... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1530... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0730 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0720 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0730 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0725 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0720 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0330 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Brand Name: CleverCut Product Name: Single Use 3-Lumen Sphincterotome V ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.