Recalls distributed in Texas – page 16

• 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
• Conductivity Standard Solution recall
  FDA February 4, 2026 · NIPRO Technical Services, Inc. · Class II
• PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recall
  FDA February 4, 2026 · Cerapedics, Inc. · Class II
• Goldenroot Yuzu Ginger Lemongrass Ginger Beer recall
  FDA February 4, 2026 · Weaver's Brew LLC · Class II
• Goldenroot Lemon Ginger Jalapeno Ginger Beer recall
  FDA February 4, 2026 · Weaver's Brew LLC · Class II
• Goldenroot Lemon Ginger Hibiscus Ginger Beer recall
  FDA February 4, 2026 · Weaver's Brew LLC · Class II
• Goldenroot Lemon Double Ginger, Ginger Beer recall
  FDA February 4, 2026 · Weaver's Brew LLC · Class II
• Goldenroot Lemon Ginger Elderberry Ginger Beer recall
  FDA February 4, 2026 · Weaver's Brew LLC · Class II
• HIGHER HARVEST by H-E-B brand recall
  FDA February 4, 2026 · Plant Based Innovations, LLC · Class II
• Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap… recall
  FDA February 4, 2026 · Quten Research Institiute LLC · Class II
• SQ40S Blood Transfusion Filter recall
  FDA January 28, 2026 · GVS TM, Inc · Class II
• EDAN Product Name: Telemetry Transmitter Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Patient Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Vital Signs Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Vital Signs Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Central Monitoring System Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Central Monitoring System Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Patient Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Patient Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Patient Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Patient Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Patient Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Vital Signs Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Vital Signs Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Vital Signs Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Fetal & Maternal Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · Class II
• EDAN Product Name: Fetal Monitor Model recall
  FDA January 28, 2026 · Edan Diagnostics · 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
• MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model recall
  FDA January 28, 2026 · MicroPort Orthopedics Inc. · Class II
• LEASEIR Product Name: LEASEIR MHR XCELL Model recall
  FDA January 28, 2026 · Leaseir Technologies Slu · 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
• MEAL SIMPLE RED LENTIL DAL SOUP NET WT. 16 OZ (1 LB) 454g recall
  FDA January 28, 2026 · Bakkavor · Class II
• White Castle Original Sliders, Net Wt recall
  FDA January 28, 2026 · White Castle System · Class I
• Portex Spinal Tray, Item No recall
  FDA January 21, 2026 · ICU Medical, Inc. · Class II
• Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2… recall
  FDA January 21, 2026 · ICU Medical, Inc. · Class II
• CentriMag Blood Pump recall
  FDA January 21, 2026 · Thoratec LLC · Class II
• da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073… recall
  FDA January 21, 2026 · Intuitive Surgical, Inc. · Class II
• The product is used for the evaluation of the intrinsic coagulation… recall
  FDA January 21, 2026 · Instrumentation Laboratory · Class II
• Catalyst+ Product Name: Catalyst, Catalyst+ Model recall
  FDA January 21, 2026 · C-Rad Positioning Ab · Class II
• MOSAIQ Oncology Information System with Particle Therapy License (License… recall
  FDA January 21, 2026 · Elekta, Inc. · Class II
• Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005 recall
  FDA January 21, 2026 · Fresenius Kabi USA, LLC · Class II
• Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter, 4F… recall
  FDA January 21, 2026 · Boston Scientific Corporation · Class II
• Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography… recall
  FDA January 21, 2026 · Mobius Imaging, LLC · Class II
• Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography… recall
  FDA January 21, 2026 · Mobius Imaging, LLC · Class II
• Medicrea, IB3D PL Instruments Set, Rx Only recall
  FDA January 21, 2026 · Medicrea International · Class II
• Medicrea, IB3D Universal Implant Inserter, Rx Only recall
  FDA January 21, 2026 · Medicrea International · Class II