Home / Brands / Olympus Corporation of the Americas
Olympus Corporation of the Americas Recalls
414 recalls on record · October 7, 2015 to July 29, 2026 · Medical Devices
Recalls by year
15
16
17
18
19
20
21
22
23
24
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls BRONCHOVIDEOSCOPE OLYMPUS BF-Q170
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls BRONCHOVIDEOSCOPE OLYMPUS BF-H1100
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
October 22, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150
Hazard: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
September 17, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019. The ViziShot 2 FLEX tissue biopsy device
Hazard: Potential for undetected, deformed a-traumatic tips.
August 27, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410. Model Number: WA91307C.
Hazard: Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.
August 27, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410 Surgical Energy Platform (SE
Hazard: Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Cone with Male Tubing, Non-Locking, Ellik Evacuator. Model Number: 191-NRS. The Ellik Evacuator and adapter accessor
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Ellik Evacuator Adapter, Locking. Model Number: 190-NRS. The Ellik Evacuator and adapter accessories are compatible
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Ellik Latex Bulb, Ellik Evacuator. Model Number: 194-2. The Ellik Evacuator and adapter accessories are compatible w
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Tubing for Male Connector 194, Ellik Evacuator. Model Number: 190-4. The Ellik Evacuator and adapter accessories are
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and adapter accessories are compatible w
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR. Model Number: CS-G7. The reusable silicone se
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Blue Silicone, Reusable Silicone Seal 6 - 12 FR. Model Number: CS-B612. The reusable silicone seals fit over the b
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).