Medical devices recalls – page 69

• Check=Flo Performer Introducer, 14.0Fr, Reference Part Number(RPN) recall
  FDA May 28, 2025 · Cook Incorporated · Class II
• Check=Flo Performer Introducer, 10.0Fr, Reference Part Number(RPN) recall
  FDA May 28, 2025 · Cook Incorporated · Class II
• True 3D Viewer, Model: EP-00003 recall
  FDA May 28, 2025 · Echopixel, Inc. · Class II
• Baxter Novum IQ LVP INFUSION SYSTEM recall
  FDA May 28, 2025 · Baxter Healthcare Corporation · Class I
• Centerline Biomedical IOPS Guidewire 2 recall
  FDA May 28, 2025 · Centerline Biomedical Inc · Class I
• 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
• Endopath Echelon Vascular White Reload for Advanced Placement Tip (35mm… recall
  FDA May 28, 2025 · Ethicon Endo Surgery, 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
• KliniTray Platte Faxitron ,groB "R" sterile recall
  FDA May 21, 2025 · Klinika Mdical Gmb · Class II
• KliniTray recall
  FDA May 21, 2025 · Klinika Mdical Gmb · Class II
• Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395 recall
  FDA May 21, 2025 · Medline Industries, LP · Class II
• Centurion Sterile Weitlaner Retractor, Reorder: 67315 recall
  FDA May 21, 2025 · Medline Industries, LP · Class II
• CMS8000 Patient Monitor recall
  FDA May 21, 2025 · Contec Medical Systems Co., Ltd. · Class II
• LifeShield Drug Library Management (DLM), LifeShield Infusion Safety… recall
  FDA May 21, 2025 · ICU Medical, Inc. · Class II
• Tornado Embolization Microcoil, intended for embolization of selective… recall
  FDA May 21, 2025 · Cook Incorporated · Class II
• Augmedics Perc Pin Adaptor, Model recall
  FDA May 21, 2025 · Augmedics Ltd. · Class II
• BIB Balloon in Balloon Dilatation Catheter recall
  FDA May 21, 2025 · Numed Inc · 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
• Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096… recall
  FDA May 21, 2025 · Abbott Molecular, Inc. · Class II
• Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090… recall
  FDA May 21, 2025 · Abbott Molecular, Inc. · Class II
• FoundationOne Companion Diagnostic (F1CDx) recall
  FDA May 21, 2025 · Foundation Medicine, Inc. · Class II
• Contour Product Name: Contour Gold Eyelid Weight Model recall
  FDA May 21, 2025 · Meddev Corp · Class II
• Contour Product Name: Contour Gold Eyelid Weight Model recall
  FDA May 21, 2025 · Meddev Corp · Class II
• Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit recall
  FDA May 21, 2025 · AVID Medical, Inc. · Class II
• Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit recall
  FDA May 21, 2025 · AVID Medical, Inc. · Class II
• Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit recall
  FDA May 21, 2025 · AVID Medical, Inc. · Class II
• MedicaLyte Liquid Bicarbonate Concentrate recall
  FDA May 21, 2025 · Nipro Renal Soultions USA, Corporation · Class I
• iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator… recall
  FDA May 21, 2025 · Medical Depot Inc. · Class I
• Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004 recall
  FDA May 21, 2025 · Baxter Healthcare Corporation · Class I
• Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002 recall
  FDA May 21, 2025 · Baxter Healthcare Corporation · Class I
• AirLife Product Name: AirLife Infant Heated Wire Circuit Model recall
  FDA May 21, 2025 · Vyaire Medical · Class I
• AirLife Product Name: AirLife Infant Heated Wire Circuit Model recall
  FDA May 21, 2025 · Vyaire Medical · Class I
• IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x recall
  FDA May 14, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Atalante X, Powered Exoskeleton recall
  FDA May 14, 2025 · Wandercraft Sas · Class II
• Blueprint Software, BPUE001. Intended for use by surgeons as a pre… recall
  FDA May 14, 2025 · Tornier S.A.S. · Class II
• 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