Recalls distributed in Vermont – page 4

• MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer… recall
  FDA February 25, 2026 · Stryker Corporation · Class II
• MONARCH Platform, Bronchoscopy recall
  FDA February 25, 2026 · Auris Health, Inc · Class II
• Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue… recall
  FDA February 25, 2026 · Bard Peripheral Vascular Inc · Class II
• Spectral CT 7500 on Rails recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Spectral CT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• IQon Spectral CT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Brilliance iCT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• MiniMed 780G Insulin Pump recall
  FDA February 11, 2026 · Medtronic MiniMed, 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
• Ingenia 3.0T CX. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia 1.5T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Evolution Upgrade 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Evolution Upgrade 1.5T. Product Codes ( recall
  FDA February 4, 2026 · Philips North America Llc · 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
• BD Pyxis ES Enterprise Server recall
  FDA January 14, 2026 · CareFusion 303, Inc. · Class II
• MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy peel shell on… recall
  FDA January 14, 2026 · Direct Source Seafood LLC · Class II
• waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal… recall
  FDA January 14, 2026 · Direct Source Seafood LLC · Class II
• Town Food Service EQ CO Inc recall
  FDA January 14, 2026 · Town Food Service Equip Co Inc · Class II
• Philips EPIQ Ultrasound Systems (various models) used in conjunction with… recall
  FDA January 7, 2026 · Philips Ultrasound, Inc · Class II
• BD Pyxis MedStation ES recall
  FDA December 31, 2025 · CareFusion 303, Inc. · Class II
• Alinity ci-series System Control Module (SCM) recall
  FDA December 24, 2025 · Abbott Laboratories · Class II
• InPen App, Model/CFN Number: MMT-8061 (Android Users) recall
  FDA December 24, 2025 · Medtronic MiniMed, Inc. · Class II
• Intelerad InteleShare software, with ProViewer component recall
  FDA December 24, 2025 · DICOM Grid, Inc. · Class II
• Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841 recall
  FDA December 10, 2025 · Philips Ultrasound, Inc · Class II
• Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt recall
  FDA December 10, 2025 · Genepro Protein, Inc. · Class I
• Costco Item# 11444 Kirkland Signature Chicken Sandwich with Caesar Salad… recall
  FDA December 10, 2025 · Costco Wholesale Corporation · Class II
• Costco Item# 19927 Kirkland Signature Caesar Salad, refrigerated… recall
  FDA December 10, 2025 · Costco Wholesale Corporation · Class II
• Cold Form Wrap: Back recall
  FDA December 3, 2025 · Djo, LLC · Class II
• CareLink Clinic recall
  FDA December 3, 2025 · Medtronic MiniMed, Inc. · Class II
• CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description recall
  FDA December 3, 2025 · Alcon Research LLC · Class II
• MONARCH Bronchoscope recall
  FDA November 26, 2025 · Auris Health, Inc · Class II
• REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer… recall
  FDA November 26, 2025 · Cellavision AB · Class II
• OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control… recall
  FDA November 26, 2025 · Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC · Class III
• Rockport Lobser Bisque recall
  FDA November 26, 2025 · Plenus Group Inc. · Class I
• Tense-X. Package: 175cc HDPE Bottle recall
  FDA November 19, 2025 · Professional Botanicals, Inc. · Class II
• Total Comfort recall
  FDA November 19, 2025 · Professional Botanicals, Inc. · Class II
• Nutra Calm Package: 175cc HDPE Bottle recall
  FDA November 19, 2025 · Professional Botanicals, Inc. · Class II
• Tandem Mobi Insulin Pump: Description recall
  FDA November 12, 2025 · Tandem Diabetes Care, Inc. · Class I
• Fusia Asian Inspirations brand Veggie Spring Rolls recall
  FDA November 5, 2025 · Tai Foong USA Inc · Class I
• Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump"… recall
  FDA October 29, 2025 · Cardinal Health 200, LLC · Class II
• Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump"… recall
  FDA October 29, 2025 · Cardinal Health 200, LLC · Class II
• Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump"… recall
  FDA October 29, 2025 · Cardinal Health 200, LLC · Class II
• Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump… recall
  FDA October 29, 2025 · Cardinal Health 200, LLC · Class II
• Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump"… recall
  FDA October 29, 2025 · Cardinal Health 200, LLC · Class II
• Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM… recall
  FDA October 29, 2025 · Cardinal Health 200, LLC · Class II