Recalls distributed in Georgia – page 27

• SmartPath to Ingenia Elition X recall
  FDA May 28, 2025 · Philips North America Llc · Class II
• SmartPath to dStream for XR and 3.0T recall
  FDA May 28, 2025 · Philips North America Llc · Class II
• SmartPath to dStream for 3.0T recall
  FDA May 28, 2025 · Philips North America Llc · Class II
• SmartPath to dStream for 1.5T recall
  FDA May 28, 2025 · Philips North America Llc · Class II
• Bard¿ Single Intragastric Linton Balloon Tube recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Bard Blakemore Esophageal-Nasogastric Tube (Adult) recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Bard Minnesota Four Lumen Esophagogastric Tamponade Tube recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Yellowstone Brown Sugar Molasses Baked Beans, NET WT… recall
  FDA May 28, 2025 · Vietti Acquisitions, LLC · Class I
• DxC 500 AU Clinical Chemistry Analyzer recall
  FDA May 21, 2025 · Beckman Coulter, Inc. · Class II
• SmartPath to dStream for 3.0T, Model Number: 782145 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• SmartPath to dStream for 1.5T, Model Number: 782146 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera CV, Model Number: 781107 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 3.0T Quasar Dual, Model Number: 781150 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.5T R11, Model Number: 781170 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.5T Power/Pulsar, Model Number: 781105 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.5T Omni/Stellar, Model Number: 781104 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.5T Master/Nova, Model Number: 781106 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.5T Explorer/Nova Dual, Model Number: 781108 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.5T, Model Numbers: 781195 and 781295 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.0T Power/Pulsar, Model Number: 781103 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.0T Omni/Stellar, Model Number: 781102 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 0.5T Standard, Model Number: 781101 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Enterprise 1.5T, Model Number: 781145 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• PiezoWave 2 Control Unit, Product Number 100506US… recall
  FDA May 21, 2025 · Richard Wolf GmbH · Class II
• Pruitt Irrigation Occlusion Catheter recall
  FDA May 21, 2025 · LeMaitre Vascular, Inc. · Class II
• Pruitt Occlusion Catheter recall
  FDA May 21, 2025 · LeMaitre Vascular, Inc. · Class II
• TufTex Over-the-Wire Embolectomy Catheter recall
  FDA May 21, 2025 · LeMaitre Vascular, Inc. · Class II
• FoundationOne Companion Diagnostic (F1CDx) recall
  FDA May 21, 2025 · Foundation Medicine, Inc. · Class II
• MedicaLyte Liquid Bicarbonate Concentrate recall
  FDA May 21, 2025 · Nipro Renal Soultions USA, Corporation · Class I
• Introducer Kit- Tearaway MicroSlide recall
  FDA May 14, 2025 · Galt Medical Corporation · Class II
• Introducer Needle recall
  FDA May 14, 2025 · Galt Medical Corporation · Class II
• Introducer Kit- Coaxial Dilator recall
  FDA May 14, 2025 · Galt Medical Corporation · Class II
• GALT Guidewire recall
  FDA May 14, 2025 · Galt Medical Corporation · Class II
• B Braun Interventional ELITE HV Hemostasis Valve Introducer System recall
  FDA May 14, 2025 · Galt Medical Corporation · Class II
• B Braun Interventional Coaxial Dilator recall
  FDA May 14, 2025 · Galt Medical Corporation · Class II
• GALT Centeze Catheter recall
  FDA May 14, 2025 · Galt Medical Corporation · Class II
• Philips Tempus Pro Patient Monitor recall
  FDA May 14, 2025 · Remote Diagnostic Technologies Ltd. · Class II
• Artix MT Thrombectomy Device recall
  FDA May 14, 2025 · Inari Medical - Oak Canyon · Class II
• Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set recall
  FDA May 14, 2025 · Ambu · Class II
• Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as… recall
  FDA May 14, 2025 · Philips North America Llc · Class II
• Enhanced Verify Evaluation Handset (CFN HH90130FA) recall
  FDA May 7, 2025 · Medtronic Neuromodulation · Class II
• myQA iON recall
  FDA May 7, 2025 · IBA Dosimetry GmbH · Class II
• Tibial Augment recall
  FDA May 7, 2025 · Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
• L-Shaped Femoral Augment recall
  FDA May 7, 2025 · Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
• Posterior Femoral Augment recall
  FDA May 7, 2025 · Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
• Distal Femoral Augment recall
  FDA May 7, 2025 · Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
• Quantum Informatics - VISION / LIVE VUE Product Name: Monitor… recall
  FDA May 7, 2025 · Spectrum Medical Ltd. · Class II
• Quantum Informatics - VIPER Product Name: Monitor, Physiological… recall
  FDA May 7, 2025 · Spectrum Medical Ltd. · Class II
• 3.0 Liter Disposable Set (4 sets/case) recall
  FDA May 7, 2025 · Belmont Instrument LLC · Class II
• DxC 500 AU Clinical Chemistry Analyzer recall
  FDA May 7, 2025 · Beckman Coulter, Inc. · Class II
• Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP… recall
  FDA April 30, 2025 · Remote Diagnostic Technologies Ltd. · Class II
• Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090… recall
  FDA April 30, 2025 · Radiometer Medical ApS · Class II
• CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
  FDA April 30, 2025 · Abbott Laboratories · Class II
• CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
  FDA April 30, 2025 · Abbott Laboratories · Class II
• CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
  FDA April 30, 2025 · Abbott Laboratories · Class II
• CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
  FDA April 30, 2025 · Abbott Laboratories · Class II
• CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
  FDA April 30, 2025 · Abbott Laboratories · Class II
• InPen smart insulin pen recall
  FDA April 30, 2025 · Medtronic MiniMed, Inc. · Class II