Recalls distributed in New Jersey – page 11

• 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
• 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
• Da Vinci Product Name: da Vinci X, Xi Surgical System… recall
  FDA February 11, 2026 · Intuitive Surgical, Inc. · Class II
• COULTER DxH Diluent recall
  FDA February 11, 2026 · Beckman Coulter, Inc. · Class II
• 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
• Conductivity Standard Solution recall
  FDA February 4, 2026 · NIPRO Technical Services, Inc. · Class II
• PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recall
  FDA February 4, 2026 · Cerapedics, Inc. · Class II
• Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap… recall
  FDA February 4, 2026 · Quten Research Institiute LLC · Class II
• 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
• Allwell Angioplasty Pack recall
  FDA January 28, 2026 · Merit Medical Systems, Inc. · Class II
• Merit Medical , Custom Procedure Kit Reference Numbers: K12T-04270A… recall
  FDA January 28, 2026 · Merit Medical Systems, Inc. · Class II
• Merit Medical , Custom Manifold Kit recall
  FDA January 28, 2026 · Merit Medical Systems, Inc. · Class II
• Merit Medical , Custom Inflation Kit recall
  FDA January 28, 2026 · Merit Medical Systems, Inc. · Class II
• Merit Medical , Custom Waste Management Kit Vascular Tray recall
  FDA January 28, 2026 · Merit Medical Systems, Inc. · Class II
• Allwell Inflation Device, for angiographic use recall
  FDA January 28, 2026 · Merit Medical Systems, Inc. · Class II
• Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference… recall
  FDA January 28, 2026 · Merit Medical Systems, Inc. · Class II
• Tego Connector recall
  FDA January 28, 2026 · ICU Medical, Inc. · Class II
• Portex Spinal Tray, Item No recall
  FDA January 21, 2026 · ICU Medical, Inc. · Class II
• Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2… recall
  FDA January 21, 2026 · ICU Medical, Inc. · Class II
• CentriMag Blood Pump recall
  FDA January 21, 2026 · Thoratec LLC · Class II