Recalls distributed in South Dakota – page 5

• 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
• 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
• MiniMed 780G Insulin Pump recall
  FDA February 11, 2026 · Medtronic MiniMed, Inc. · Class II
• COULTER DxH Diluent recall
  FDA February 11, 2026 · Beckman Coulter, Inc. · Class II
• Repackaged M&Ms candies, Net Wt 1.3 oz recall
  FDA February 11, 2026 · Beacon Promotions Inc · Class II
• Repackaged M&Ms Peanut candies, Net Wt 1.3 oz recall
  FDA February 11, 2026 · Beacon Promotions Inc · Class II
• JUICE from the Raw, cashew coffee milk recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, cashew milk recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, spicy lemonade recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, upbeat recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, pineapple mint recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, sweet greens recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, DETOX GREENS recall
  FDA February 11, 2026 · Everpress Juice · Class I
• The LDL-Cholesterol assay is comprised of two distinct phases recall
  FDA January 28, 2026 · Beckman Coulter Ireland, Inc. · Class II
• Ion Endoluminal System Product Name: Ion Vision Probe Bag Model recall
  FDA January 28, 2026 · Intuitive Surgical, Inc. · Class II
• Tego Connector recall
  FDA January 28, 2026 · ICU Medical, Inc. · Class II
• da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073… recall
  FDA January 21, 2026 · Intuitive Surgical, Inc. · Class II
• FreeStyle Libre 3 Plus Sensor recall
  FDA January 21, 2026 · Abbott Diabetes Care, Inc. · Class I
• FreeStyle Libre 3 Plus Sensor recall
  FDA January 21, 2026 · Abbott Diabetes Care, Inc. · Class I
• FreeStyle Libre 3 Plus Sensor recall
  FDA January 21, 2026 · Abbott Diabetes Care, Inc. · Class I
• FreeStyle Libre 3 Sensor recall
  FDA January 21, 2026 · Abbott Diabetes Care, Inc. · Class I
• Codman CereLink ICP Sensor Basic Kit recall
  FDA January 14, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• Codman Microsensor Basic Kit recall
  FDA January 14, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II