Class IOngoingZ-2484-2025
Olympus Corporation Of The Americas recalls ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019. The Vizi…
Potential for undetected, deformed a-traumatic tips.
Olympus Corporation of…PASep 17, 2025
Olympus Corporation of the Americas recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 133–144 of 163 recalls
Class IIOngoingZ-2339-2025
Olympus Corporation Of The Americas recalls Electrosurgical
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'.
Olympus Corporation of…PAAug 27, 2025
Class IIOngoingZ-2338-2025
Olympus Corporation Of The Americas recalls Electrosurgical
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'.
Olympus Corporation of…PAAug 27, 2025
Class IIOngoingZ-2146-2025
Olympus Corporation Of The Americas recalls Cone with Male Tubing
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2145-2025
Olympus Corporation Of The Americas recalls Ellik Evacuator Adapter
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2144-2025
Olympus Corporation Of The Americas recalls Ellik Latex Bulb
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2143-2025
Olympus Corporation Of The Americas recalls Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are…
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2142-2025
Olympus Corporation Of The Americas recalls Tubing for Male Connector 194
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2141-2025
Olympus Corporation Of The Americas recalls Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and ada…
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2140-2025
Olympus Corporation Of The Americas recalls Green Silicone Seal for Accessories
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-2139-2025
Olympus Corporation Of The Americas recalls Blue Silicone
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of…PAJul 30, 2025
Class IIOngoingZ-1923-2025
Olympus Corporation Of The Americas recalls Brand Name: Powered Laser Surgical Instrument Product Name: Soltive Reusable Laser Fib…
Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use.…
Olympus Corporation of…PAJun 18, 2025