Recalls distributed in Texas – page 14

• Prodisc Product Name: Prodisc C SK Model recall
  FDA February 25, 2026 · Centinel Spine, Inc. · 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
• Private Label CVS. Model Number: CVS405406… recall
  FDA February 25, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY… recall
  FDA February 25, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney Gel with Active Leptospermum Honey recall
  FDA February 25, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep… recall
  FDA February 25, 2026 · Pure Solutions, Inc. · Class II
• Barco MNA with the HexaVue IP Integration System, Model recall
  FDA February 18, 2026 · Steris Corporation · Class II
• Surepulse VS Cap Extra Large recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• Surepulse VS Cap Large recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• Surepulse VS Cap Medium recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• Surepulse VS Cap Small recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• Surepulse VS Cap Extra Small recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000… recall
  FDA February 18, 2026 · Intuitive Surgical, Inc. · Class II
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm recall
  FDA February 18, 2026 · Alphatec Spine, Inc. · Class II
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm recall
  FDA February 18, 2026 · Alphatec Spine, Inc. · Class II
• Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
  FDA February 18, 2026 · Elekta, Inc. · Class II
• Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
  FDA February 18, 2026 · Elekta, 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
• CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g)… recall
  FDA February 18, 2026 · Ventura Foods LLC · Class II
• CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/GRAPE JELLY NET WT 1 OZ (28g)… recall
  FDA February 18, 2026 · Ventura Foods LLC · Class II
• CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS… recall
  FDA February 18, 2026 · Ventura Foods 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
• 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
• Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel… recall
  FDA February 18, 2026 · Costco Wholesale Corporation · Class I
• 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