Nationwide recalls – page 44

• 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
• Vivoo Sodium Test recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• Vivoo Vaginal pH Test recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• Vivoo Protein Test recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• Vivoo pH Test recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• Exploro Highly Sensitive Male Fertility / Sperm Concentration Test recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• Male Fertility Sperm Test for Home Use (Cassette) recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• S. Typhi/Para Typhi A Antigen recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• Menopause Test Cassette (Urine) recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• LH One Step Ovulation Test Device (Urine) recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• The Girlfriend Doctor Dr recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• LotFancy Urinary Tract Infection Urine (UTI) Test Strips recall
  FDA February 11, 2026 · Changchun Wancheng Bio-Electron Co., Ltd. · Class II
• Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical 25GA Backflush, VS0270.25 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical TID Pharos Illuminated Depressor, VS0801B recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Rumex Disposable Diamond Dusted ILM Elevator, 12-7523 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical I2 Injection Kit, VS0500 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Tecfen Retractable Membrane Polisher, QTPR1267-23 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2… recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• 25GA Subretinal Injection Cannula VS0220.25 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive… recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2… recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical 1. 23GA Laser Probe Curved Cat No recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Focalyx Fusion recall
  FDA February 11, 2026 · Focalyx Technologies, LLC. · Class II
• NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification… recall
  FDA February 11, 2026 · Siemens Medical Solutions USA, Inc · Class II
• NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification… recall
  FDA February 11, 2026 · Siemens Medical Solutions USA, Inc · Class II
• NAEOTOM Alpha Software applications: syngo.CT Brain Quantification… recall
  FDA February 11, 2026 · Siemens Medical Solutions USA, Inc · Class II
• SOMATOM X.ceed Software applications: syngo.CT Brain Quantification… recall
  FDA February 11, 2026 · Siemens Medical Solutions USA, Inc · Class II
• TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE… recall
  FDA February 11, 2026 · Tornier, Inc · Class II
• VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B… recall
  FDA February 11, 2026 · Biomerieux Inc · Class II
• CellMek SPS Sample Preparation System recall
  FDA February 11, 2026 · Beckman Coulter, Inc. · Class II
• PRISMAFLEX TPE2000 SET, Product Code 114093 recall
  FDA February 11, 2026 · Vantive Us Healthcare LLC · Class II
• PRISMAFLEX HF1000 SET, Product Code 107142 recall
  FDA February 11, 2026 · Vantive Us Healthcare LLC · Class II
• PRISMAFLEX HF1000 SET, Product Code 107140 recall
  FDA February 11, 2026 · Vantive Us Healthcare LLC · Class II
• PRISMAFLEX M150 SET, Product Code 109990 recall
  FDA February 11, 2026 · Vantive Us Healthcare LLC · Class II
• PRIMSAFLEX M100 SET, Product Code 106697 recall
  FDA February 11, 2026 · Vantive Us Healthcare LLC · Class II
• OXIRIS SET, Product Code 112016 recall
  FDA February 11, 2026 · Vantive Us Healthcare LLC · Class II
• PRISMAFLEX ST150 SET US, Product Code 107640US recall
  FDA February 11, 2026 · Vantive Us Healthcare LLC · Class II
• PRISMAFLEX ST100 SET US, Product Code 107636US recall
  FDA February 11, 2026 · Vantive Us Healthcare LLC · 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
• COULTER DxH Diluent recall
  FDA February 11, 2026 · Beckman Coulter, Inc. · Class II
• *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm recall
  FDA February 11, 2026 · Boston Scientific Corporation · Class I
• *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm recall
  FDA February 11, 2026 · Boston Scientific Corporation · Class I
• HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm recall
  FDA February 11, 2026 · Boston Scientific Corporation · Class I
• AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm recall
  FDA February 11, 2026 · Boston Scientific Corporation · Class I
• AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm recall
  FDA February 11, 2026 · Boston Scientific Corporation · Class I
• AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm recall
  FDA February 11, 2026 · Boston Scientific Corporation · Class I