Medical devices recalls – page 73

• Ballard Product Name: Closed Suction Catheters Model recall
  FDA April 23, 2025 · Avanos Medical, Inc. · Class I
• Ballard Product Name: Closed Suction Catheters Model recall
  FDA April 23, 2025 · Avanos Medical, Inc. · Class I
• Ballard Product Name: Closed Suction Catheters Model recall
  FDA April 23, 2025 · Avanos Medical, Inc. · Class I
• Tandem Mobi Insulin Pump with Interoperable Technology recall
  FDA April 23, 2025 · Tandem Diabetes Care, Inc. · Class I
• t:slim X2 Insulin Pump with Interoperable Technology recall
  FDA April 23, 2025 · Tandem Diabetes Care, Inc. · Class I
• BD 4 Fr Single-Lumen PowerPICC Catheters recall
  FDA April 23, 2025 · Bard Access Systems, Inc. · Class I
• Atellica CH Revised C Reactive Protein (RCRP) recall
  FDA April 16, 2025 · Siemens Healthcare Diagnostics, Inc. · Class II
• BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID BD… recall
  FDA April 16, 2025 · CareFusion 303, Inc. · Class II
• MEDLINE ReNewal ENT Coblator II PROcise mAx,W/ Integrated Cable Suction &… recall
  FDA April 16, 2025 · Medline Industries, LP · Class II
• MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction… recall
  FDA April 16, 2025 · Medline Industries, LP · Class II
• MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP,w/Integrated Cable… recall
  FDA April 16, 2025 · Medline Industries, LP · Class II
• MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand,w/Integrated Saline… recall
  FDA April 16, 2025 · Medline Industries, LP · Class II
• BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex… recall
  FDA April 16, 2025 · CareFusion 303, Inc. · Class II
• GenetiSure Dx Labeling Kit recall
  FDA April 16, 2025 · Agilent Technologies, Inc. · Class II
• Stimulation RC Clinician Programmer Application, Model A71400… recall
  FDA April 16, 2025 · Medtronic Neuromodulation · Class II
• stryker HoloBlueprint Application recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• stryker Blueprint Mixed Reality Instrument Kit recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• stryker Blueprint Mixed Reality Depth Stop Pin recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• stryker Blueprint Mixed Reality Glenoid Box Lid recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• stryker Blueprint Mixed Reality Box Base recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• stryker Blueprint Mixed Reality Instrument Check Block recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• stryker Blueprint Mixed Reality Coracoid Clamp recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• stryker Blueprint Mixed Reality Glenoid Digitizer recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless… recall
  FDA April 16, 2025 · Tornier S.A.S. · Class II
• IVX Station Reconstitution Transfer Set recall
  FDA April 16, 2025 · Omnicell, Inc. · Class II
• Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT… recall
  FDA April 16, 2025 · Medline Industries, LP · Class II
• Wayson Hydrocolloid Models: 1) Model Number: CUR5103… recall
  FDA April 16, 2025 · Medline Industries, LP · Class II
• DxI 9000 Access Immunoassay Analyzer, catalog number C11137 in vitro… recall
  FDA April 16, 2025 · Beckman Coulter, Inc. · Class II
• FilmArra Pneumonia Panel plus (Pneumoplus) recall
  FDA April 16, 2025 · BioFire Diagnostics, LLC · Class II
• Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration… recall
  FDA April 16, 2025 · Qapel Medical Inc. · Class I
• Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY recall
  FDA April 16, 2025 · Medline Industries, LP · Class I
• Medline medical procedure kits, containing Medtronic Aortic Root Cannula… recall
  FDA April 16, 2025 · Medline Industries, LP · Class I
• Medline medical procedure kits, containing Medtronic Aortic Root Cannula… recall
  FDA April 16, 2025 · Medline Industries, LP · Class I
• Medline medical procedure kits, containing Medtronic Aortic Root Cannula… recall
  FDA April 16, 2025 · Medline Industries, LP · Class I
• Medline medical procedure kits, containing Medtronic Aortic Root Cannula… recall
  FDA April 16, 2025 · Medline Industries, LP · Class I
• DxC 500 AU Clinical Chemistry Analyzer recall
  FDA April 9, 2025 · Beckman Coulter, Inc. · Class II
• ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH recall
  FDA April 9, 2025 · Ethicon Endo Surgery, LLC · Class II
• PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM recall
  FDA April 9, 2025 · Ethicon Endo Surgery, LLC · Class II
• PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 recall
  FDA April 9, 2025 · Ethicon Endo Surgery, LLC · Class II
• PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP recall
  FDA April 9, 2025 · Ethicon Endo Surgery, LLC · Class II
• Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC… recall
  FDA April 9, 2025 · Cordis US Corp · Class II
• Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC… recall
  FDA April 9, 2025 · Cordis US Corp · Class II
• BD Connecta BD Luer-Lok 360 recall
  FDA April 9, 2025 · Bd Switzerland Sarl · Class II
• Boppli: Bedside Device Kit recall
  FDA April 9, 2025 · Pyrames Inc · Class II
• A820 myPTM Software Application associated with Medtronic SynchroMed Pump… recall
  FDA April 9, 2025 · Medtronic Neuromodulation · Class II
• QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference… recall
  FDA April 9, 2025 · Qiagen Sciences LLC · Class II
• Pacific Hemostasis Thromboplastin-D, 10 ml recall
  FDA April 9, 2025 · Fisher Diagnostics · Class II
• Pacific Hemostasis Thromboplastin-D, 4 ml recall
  FDA April 9, 2025 · Fisher Diagnostics · Class II
• Phoroptor VRx Digital Refraction System Model Numbers: 16242 recall
  FDA April 9, 2025 · Reichert, Inc. · Class II
• Phoroptor VRx Digital Refraction System Model Numbers: 16241 recall
  FDA April 9, 2025 · Reichert, Inc. · Class II
• Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model recall
  FDA April 9, 2025 · Draeger, Inc. · Class I
• Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model recall
  FDA April 9, 2025 · Draeger, Inc. · Class I
• Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model recall
  FDA April 9, 2025 · Draeger, Inc. · Class I
• Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model recall
  FDA April 9, 2025 · Draeger, Inc. · Class I
• Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model recall
  FDA April 9, 2025 · Draeger, Inc. · Class I
• ID Circuit Product Name: ID Circuit Flex 220 Model recall
  FDA April 9, 2025 · Draeger, Inc. · Class I
• VentStar Product Name: VentStar Flex 220 Model recall
  FDA April 9, 2025 · Draeger, Inc. · Class I
• Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe recall
  FDA April 9, 2025 · Terumo Cardiovascular Systems Corporation · Class II
• Monterey AL Implant Inserter recall
  FDA April 9, 2025 · Stryker Spine · Class II
• Monterey AL Implant Inserter recall
  FDA April 9, 2025 · Stryker Spine · Class II