Medical devices recalls – page 80

• Cardinal Health Presource Kits: 1) KIT,DIEP FLAP recall
  FDA February 19, 2025 · Cardinal Health 200, LLC · Class II
• BD Pyxis MedStation 4000 recall
  FDA February 19, 2025 · CareFusion 303, Inc. · Class II
• BD Pyxis MedStation Auxiliary 4000 recall
  FDA February 19, 2025 · CareFusion 303, Inc. · Class II
• BD Pyxis MedStation Auxiliary ES recall
  FDA February 19, 2025 · CareFusion 303, Inc. · Class II
• BD Pyxis MedStation ES (Med ES Main) recall
  FDA February 19, 2025 · CareFusion 303, Inc. · Class II
• MicoVention Terumo, LVIS Intraluminal Support Device recall
  FDA February 19, 2025 · Microvention Inc. · Class II
• (1) BD Pyxis MedStation ES recall
  FDA February 19, 2025 · CareFusion 303, Inc. · Class II
• (1) Pyxis MedStation ES recall
  FDA February 19, 2025 · CareFusion 303, Inc. · Class II
• Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use… recall
  FDA February 19, 2025 · Max Mobility LLC · Class I
• Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use… recall
  FDA February 19, 2025 · Max Mobility LLC · Class I
• The MSOT Acuity Echo is a Class 4 medical laser device recall
  FDA February 19, 2025 · Ithera Medical Gmbh · Class II
• Vaporizer Sevoflurane, Quik-Fil recall
  FDA February 19, 2025 · Getinge Usa Sales Inc · Class I
• Olympus Single Use Guide Sheath Kits with the following product… recall
  FDA February 19, 2025 · Olympus Corporation of the Americas · Class I
• UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number… recall
  FDA February 12, 2025 · Medicrea International · Class II
• Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137 recall
  FDA February 12, 2025 · Beckman Coulter, Inc. · Class II
• Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK… recall
  FDA February 12, 2025 · US Endodontics, LLC · Class II
• Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6 recall
  FDA February 12, 2025 · Sysmex America, Inc. · Class II
• Access PCT Reagent Pack recall
  FDA February 12, 2025 · Beckman Coulter, Inc. · Class II
• Temporary Titanium Abutments recall
  FDA February 12, 2025 · DDS Lab · Class II
• IntelliVue Patient Monitor MX550. Model Number: 866066 recall
  FDA February 12, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX500. Model Number: 866064 recall
  FDA February 12, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX450. Model Number: 866062 recall
  FDA February 12, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX400. Model Number: 866060 recall
  FDA February 12, 2025 · Philips North America Llc · Class II
• IntelliBridge EC10 Module recall
  FDA February 12, 2025 · Philips North America Llc · Class II
• NeiMed NasoGel for DRY NOSES UDI-DI recall
  FDA February 12, 2025 · Neilmed Pharmaceuticals Inc · Class II
• Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each)… recall
  FDA February 12, 2025 · New Medical Technologies Gmbh · Class II
• Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each)… recall
  FDA February 12, 2025 · New Medical Technologies Gmbh · Class II
• LIFEPAK 35 ECG cable recall
  FDA February 12, 2025 · Physio-Control, Inc. · Class II
• Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Biocare N1 TiUltra TCC RP… recall
  FDA February 12, 2025 · Nobel Biocare · Class II
• Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Infuser… recall
  FDA February 12, 2025 · Belmont Instrument LLC · Class II
• ETHIBOND EXCEL Polyester Suture recall
  FDA February 12, 2025 · Ethicon, LLC · Class II
• PERMA-HAND Silk Suture recall
  FDA February 12, 2025 · Ethicon, LLC · Class II
• PROLENE Polypropylene Suture recall
  FDA February 12, 2025 · Ethicon, LLC · Class II
• The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of… recall
  FDA February 12, 2025 · Hologic, Inc · Class II
• Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282… recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M12 System Code: (1) 722227 (2) 722231 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M12 System Code: (1) 722063 (2) 722221 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXperFD20/15 System Code: (1) 722058 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/20 System Code: (1) 722038 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXperFD20/10 System Code: (1) 722029 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD10C System Code: (1) 722001 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD10 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Allura CV20 System Code: 722031 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Lev5, REF CT1587B, 50 Susceptibility discs Levofloxacin 5 ug, IVD, CE 2797 recall
  FDA February 12, 2025 · Oxoid Limited · Class II
• SenTiva, REF: 1000C, Generators Part of the VNS Therapy System with… recall
  FDA February 12, 2025 · LivaNova USA, Inc. · Class II
• SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D… recall
  FDA February 12, 2025 · LivaNova USA, Inc. · Class II
• regard Item Number: 830106006, LD01114F - Newborn Kit containing the… recall
  FDA February 12, 2025 · ROi CPS LLC · Class I
• Optima XR646 HD. X-Ray imaging system recall
  FDA February 12, 2025 · GE Medical Systems, LLC · Class II
• Discovery XR656 HD. X-Ray imaging system recall
  FDA February 12, 2025 · GE Medical Systems, LLC · Class II
• Discovery XR656HD. X-Ray imaging system recall
  FDA February 12, 2025 · GE Medical Systems, LLC · Class II