Recalls distributed in Massachusetts – page 10

• 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
• Focalyx Fusion recall
  FDA February 11, 2026 · Focalyx Technologies, LLC. · Class II
• MiniMed 780G Insulin Pump recall
  FDA February 11, 2026 · Medtronic MiniMed, Inc. · Class II
• CellMek SPS Sample Preparation System recall
  FDA February 11, 2026 · Beckman Coulter, Inc. · Class II
• EMPOWR Acetabular System: Liner, 10 degree Hooded, HXe+, 36H recall
  FDA February 11, 2026 · Encore Medical, LP · Class II
• EMPOWR 3D Knee Tibial Insert 5R 14MM, VE recall
  FDA February 11, 2026 · Encore Medical, LP · Class II
• COULTER DxH Diluent recall
  FDA February 11, 2026 · Beckman Coulter, Inc. · Class II
• Willy Pete's Chocolates brand Almond Despair recall
  FDA February 11, 2026 · Willy Pete's Chocolate Company LLC · Class III
• Imu-Tek Immuno-5 Colostrum Powder 7 oz recall
  FDA February 11, 2026 · Imu-Tek Animal Health, Incorporated · 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
• Andy & Evan Recalls Children's Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard…
  CPSC February 5, 2026 · Andy & Evan
• BEAR Implant recall
  FDA February 4, 2026 · Miach Orthopaedics · Class II
• LimFlow Vector Product Name: LimFlow Vector Model recall
  FDA February 4, 2026 · LimFlow, Inc. · Class II
• SmartPath to dStream for XR and 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• SmartPath to dStream for 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Upgrade to MR 7700. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• MR 7700. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Elition X. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Elition S. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Ambition X. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Ambition S. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II