Recalls distributed in Delaware – page 5

• 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
• 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
• GLUTEN FREE 14" SEASONED VEGAN PIZZA CRUST recall
  FDA February 11, 2026 · Rich Products Corp · Class II
• Conductivity Standard Solution recall
  FDA February 4, 2026 · NIPRO Technical Services, 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
• Philips Azurion system recall
  FDA January 28, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Tego Connector recall
  FDA January 28, 2026 · ICU Medical, Inc. · Class II
• CentriMag Blood Pump recall
  FDA January 21, 2026 · Thoratec LLC · Class II
• 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
• BD Pyxis ES Enterprise Server recall
  FDA January 14, 2026 · CareFusion 303, Inc. · Class II
• Philips Tempus Pro Patient Monitor recall
  FDA January 14, 2026 · Remote Diagnostic Technologies Ltd. · Class II
• Bengal King Jhal Chanachur food treats 12.34oz (350gm) recall
  FDA January 14, 2026 · South Asian Food Inc. · Class I
• Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid… recall
  FDA January 14, 2026 · Ambriola Co., Inc., The · Class I
• Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags… recall
  FDA January 14, 2026 · Ambriola Co., Inc., The · Class I
• Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit) recall
  FDA January 14, 2026 · Ambriola Co., Inc., The · Class I
• Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units per case recall
  FDA January 14, 2026 · Ambriola Co., Inc., The · Class I
• Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid… recall
  FDA January 14, 2026 · Ambriola Co., Inc., The · Class I
• Pinna Grated Pecorino Romano 2/10, 10-pound plastic bags (units) recall
  FDA January 14, 2026 · Ambriola Co., Inc., The · Class I
• Locatelli Grated Pecorino Romano, 5 and 10-pound plastic bags (units) recall
  FDA January 14, 2026 · Ambriola Co., Inc., The · Class I
• Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup & lid… recall
  FDA January 14, 2026 · Ambriola Co., Inc., The · Class I
• Philips EPIQ Ultrasound Systems (various models) used in conjunction with… recall
  FDA January 7, 2026 · Philips Ultrasound, Inc · Class II
• BECKMAN COULTER BICARBONATE recall
  FDA December 31, 2025 · Beckman Coulter Ireland, Inc. · Class II
• BD Pyxis MedStation ES recall
  FDA December 31, 2025 · CareFusion 303, Inc. · Class II
• Locatelli Pecorino Romano Cheese Grated (Wegmans #270010) Packaged and… recall
  FDA December 31, 2025 · Wegmans Food Markets, Inc. · Class I
• 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
• HemosIL SynthAFax recall
  FDA December 24, 2025 · Instrumentation Laboratory · Class III
• Food to Live brand ORGANIC SUPERGREENS POWDER MIX, packaged heat-sealed… recall
  FDA December 24, 2025 · Lexunder Inc · Class I
• Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed… recall
  FDA December 24, 2025 · Lexunder Inc · Class I
• DEXLOCK Achilles Repair Implant Kits, MAKT4520 recall
  FDA December 17, 2025 · Medline Industries, LP · Class II
• CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer… recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System… recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III