Recalls distributed in Kentucky – page 8

• Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case recall
  FDA March 4, 2026 · Sb Food LLC · Class II
• Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case recall
  FDA March 4, 2026 · Sb Food LLC · Class II
• MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer… recall
  FDA February 25, 2026 · Stryker Corporation · 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
• Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep… recall
  FDA February 25, 2026 · Pure Solutions, Inc. · Class II
• Woodland Gourmet Arrowroot Flour item code H59EE86, Net Wt recall
  FDA February 25, 2026 · Woodland Foods LLC · Class II
• Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
  CPSC February 19, 2026 · Meijer
• da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000… recall
  FDA February 18, 2026 · Intuitive Surgical, 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
• Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz recall
  FDA February 18, 2026 · Domino Foods Inc · Class III
• Spicy Breakfast Burrito in a flour tortilla recall
  FDA February 18, 2026 · MG Foods-Compass Group · Class II
• Sonic Tots, item number SON00543. Frozen potato product is packaged in… recall
  FDA February 18, 2026 · McCain Foods USA Inc · Class II
• Ore-Ida Tater Tots shaped potatoes, item number OIF00215A… recall
  FDA February 18, 2026 · McCain Foods USA Inc · Class II
• Lumipulse ¿-Amyloid Plasma Controls Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse pTau 217 Plasma Controls Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau 217 Plasma Calibrators Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · 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
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• 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