Olympus Corporation of the Americas recalls – page 2

• Olympus Resection Sheath, 28 Fr recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Resection Sheath, 26 Fr recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Resection Sheath, 26 Fr recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Resection Sheath, 24 Fr., with Deflecting Obturator recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Resection Sheath, 24 Fr recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Resection Inner Sheath for 26 Fr recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Resection Inner Sheath, for 26 Fr recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Resection Sheath recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Cystoscope Outer Sheath recall
  FDA March 4, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 10 cm, Inline Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 35 cm, Inline Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 45 cm Inline Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5mm, 35 cm, Pistol Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 45 cm, Pistol Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 35 cm, Front-Actuated Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 45 cm Front-Actuated Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 35 cm, Front-Actuated Grip Type S recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus High Flow Insufflation Unit recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class I
• Olympus High Flow Insufflation Unit recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class I
• Olympus High Flow Insufflation Unit recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class I
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple… recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• CleverCut Product Name: Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use Electrosurgical Knife KD-645 Product Name: Olympus Single Use… recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use Electrosurgical Knife Product Name: Olympus Single Use… recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V Model recall
  FDA December 3, 2025 · Olympus Corporation of the Americas · Class II
• Single Use Ligating Device Product Name: Olympus HX-400U-30 Model recall
  FDA December 3, 2025 · Olympus Corporation of the Americas · Class I
• EZDilate Nephrostomy Balloon Catheter and Inflation Device Kit Product… recall
  FDA November 26, 2025 · Olympus Corporation of the Americas · Class II
• Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name:… recall
  FDA November 19, 2025 · Olympus Corporation of the Americas · Class II