Medical devices recalls – page 53

• ACCOLADE SR SL (Model L300) recall
  FDA October 22, 2025 · Boston Scientific Corporation · Class I
• 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
• Zenith Alpha 2 Thoracic Endovascular Graft recall
  FDA October 22, 2025 · Cook Medical Incorporated · Class I
• Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) recall
  FDA October 22, 2025 · Percussionaire Corporation · Class I
• NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90 recall
  FDA October 15, 2025 · Applied Medical Technology Inc · Class II
• NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55 recall
  FDA October 15, 2025 · Applied Medical Technology Inc · Class II
• NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90 recall
  FDA October 15, 2025 · Applied Medical Technology Inc · Class II
• NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55 recall
  FDA October 15, 2025 · Applied Medical Technology Inc · Class II
• Design Options, PERIFIX FX Epidural Anesthesia Tray recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• Combined Spinal and Epidural Anesthesia Tray 2, PERIFIX 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• Design Options, Pain Management Tray recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• PERIFIX FX Continuous Epidural Anesthesia Set… recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• PERIFIX FX Continuous Epidural Anesthesia Tray, 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
  FDA October 15, 2025 · B Braun Medical Inc · Class II
• FlexLab X (FXX) System recall
  FDA October 15, 2025 · Inpeco S.A. · Class II
• FlexLab (FLX) System recall
  FDA October 15, 2025 · Inpeco S.A. · Class II
• Artegraft Collagen Vascular Graft recall
  FDA October 15, 2025 · LeMaitre Vascular, Inc. · Class II
• SYNCHRON Systems Phosphorus (PHOSm) Reagent recall
  FDA October 15, 2025 · Beckman Coulter, Inc. · Class II
• Automated Impella Controller (AIC), used for left heart support blood… recall
  FDA October 15, 2025 · Abiomed, Inc. · Class I
• AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2 recall
  FDA October 15, 2025 · GE Medical Systems SCS · Class II
• FDR Visionary Suite, CH-200 Model/Version Numbers: (1) 566-16130-23… recall
  FDA October 15, 2025 · FUJIFILM Healthcare Americas Corporation · Class II
• Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX… recall
  FDA October 15, 2025 · Fresenius Medical Care Holdings, Inc. · Class II
• EverPatch+ recall
  FDA October 15, 2025 · Corneat Vision, Ltd. · Class II
• CorNeat EverPatch recall
  FDA October 15, 2025 · Corneat Vision, Ltd. · Class II
• ClariTEE Miniaturized TEE probe recall
  FDA October 15, 2025 · ImaCor Inc. · Class II
• This device is a digital radiography/fluoroscopy system used in a… recall
  FDA October 15, 2025 · Canon Medical System, USA, INC. · Class II
• BD Alaris Pump Infusion Sets for the following reference numbers: C24101E… recall
  FDA October 15, 2025 · CareFusion 303, Inc. · Class I
• NOxBOXi Nitric Oxide Delivery System recall
  FDA October 15, 2025 · Noxbox Ltd · Class I
• NOxBOXi Nitric Oxide Delivery System recall
  FDA October 15, 2025 · Noxbox Ltd · Class I
• Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0… recall
  FDA October 8, 2025 · MedicalCommunications GmbH · Class II
• Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031… recall
  FDA October 8, 2025 · Schiller, Ag · Class II