Recalls distributed in Wyoming – 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 (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
• 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
• LimFlow Vector Product Name: LimFlow Vector Model recall
  FDA February 4, 2026 · LimFlow, Inc. · Class II
• PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recall
  FDA February 4, 2026 · Cerapedics, Inc. · 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
• 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
• 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
• 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
• 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
• 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
• 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
• FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer… recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• Sticker label (for Loose Bulk - peppermint peaches): 4401 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Sticker label (for Loose Bulk - peppermint peaches): 4401 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Sticker label (for Loose Bulk - white peaches): 4401 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Sticker label (for Loose Bulk - yellow peaches): 4044 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I
• Sticker label (for Loose Bulk - yellow peaches): 4044 recall
  FDA December 17, 2025 · Moonlight Packing Corporation · Class I