Olympus Corporation of the Americas recalls – page 3

• Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use… recall
  FDA November 19, 2025 · Olympus Corporation of the Americas · Class II
• Lithotriptor, Ultrasonic Product Name: ShockPulse Lithotripsy Transducer… recall
  FDA November 19, 2025 · Olympus Corporation of the Americas · Class II
• OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 recall
  FDA October 22, 2025 · Olympus Corporation of the Americas · Class I
• ViziShot 2FLEX. Single Use Aspiration Needle recall
  FDA September 17, 2025 · Olympus Corporation of the Americas · Class I
• Electrosurgical, Cutting and Coagulation and Accessories recall
  FDA August 27, 2025 · Olympus Corporation of the Americas · Class II
• Electrosurgical, Cutting and Coagulation and Accessories recall
  FDA August 27, 2025 · Olympus Corporation of the Americas · Class II
• Cone with Male Tubing, Non-Locking, Ellik Evacuator recall
  FDA July 30, 2025 · Olympus Corporation of the Americas · Class II
• Ellik Evacuator Adapter, Locking recall
  FDA July 30, 2025 · Olympus Corporation of the Americas · Class II
• Ellik Latex Bulb, Ellik Evacuator recall
  FDA July 30, 2025 · Olympus Corporation of the Americas · Class II
• Ellik Evacuator recall
  FDA July 30, 2025 · Olympus Corporation of the Americas · Class II
• Tubing for Male Connector 194, Ellik Evacuator recall
  FDA July 30, 2025 · Olympus Corporation of the Americas · Class II
• Glass Body For 194 Ellik Evacuator recall
  FDA July 30, 2025 · Olympus Corporation of the Americas · Class II
• Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR… recall
  FDA July 30, 2025 · Olympus Corporation of the Americas · Class II
• Blue Silicone, Reusable Silicone Seal 6 - 12 FR. Model Number: CS-B612… recall
  FDA July 30, 2025 · Olympus Corporation of the Americas · Class II
• Powered Laser Surgical Instrument Product Name: Soltive Reusable Laser… recall
  FDA June 18, 2025 · Olympus Corporation of the Americas · Class II
• Powered Laser Surgical Instrument Product Name: Soltive SuperPulsed Laser… recall
  FDA June 18, 2025 · Olympus Corporation of the Americas · Class II
• Powered Laser Surgical Instrument Product Name: SOLTIVE Premium… recall
  FDA June 18, 2025 · Olympus Corporation of the Americas · Class II
• Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed… recall
  FDA June 18, 2025 · Olympus Corporation of the Americas · Class II
• Olympus EVIS EXERA III Duodenovideoscope recall
  FDA June 11, 2025 · Olympus Corporation of the Americas · Class II
• Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed… recall
  FDA May 7, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Single Use Guide Sheath Kits with the following product… recall
  FDA February 19, 2025 · Olympus Corporation of the Americas · Class I
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product… recall
  FDA January 29, 2025 · Olympus Corporation of the Americas · Class II
• LithoCrushV Single Use Mechanical Lithotriptor V… recall
  FDA January 22, 2025 · Olympus Corporation of the Americas · Class II
• Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type) recall
  FDA January 22, 2025 · Olympus Corporation of the Americas · Class I
• Duravent Silicone Ventilation Tube recall
  FDA December 25, 2024 · Olympus Corporation of the Americas · Class II
• EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190… recall
  FDA December 11, 2024 · Olympus Corporation of the Americas · Class II
• EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product Name:… recall
  FDA November 27, 2024 · Olympus Corporation of the Americas · Class II
• UroPass Ureteral Access Sheaths Product Name: Ureteral Access Sheaths Model recall
  FDA November 20, 2024 · Olympus Corporation of the Americas · Class II