Class II medical devices recalls – page 61

• Medline Convenience kits used for various procedures: 1) PAIN PACK… recall
  FDA April 23, 2025 · Medline Industries, LP · Class II
• Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK… recall
  FDA April 23, 2025 · Medline Industries, LP · Class II
• Medline Convenience kits used for various procedures: 1) INTUBATION TRAY… recall
  FDA April 23, 2025 · Medline Industries, LP · Class II
• Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION… recall
  FDA April 23, 2025 · Channel Medsystems, Inc. · Class II
• Rover Product Name: Mobile X-ray System Model recall
  FDA April 23, 2025 · Micro-X Ltd. · Class II
• Rover Product Name: Mobile X-ray System Model recall
  FDA April 23, 2025 · Micro-X Ltd. · Class II
• Maquet VH-3010 Power Supply recall
  FDA April 23, 2025 · Maquet Cardiovascular, LLC · Class II
• ID NOW RSV 24T Product Name: ID NOW RSV 24T Model recall
  FDA April 23, 2025 · Abbott Diagnostics Scarborough, Inc. · Class II
• ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model recall
  FDA April 23, 2025 · Abbott Diagnostics Scarborough, Inc. · Class II
• ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model recall
  FDA April 23, 2025 · Abbott Diagnostics Scarborough, Inc. · Class II
• ID NOW RSV 24T Product Name: ID NOW RSV 24T Model recall
  FDA April 23, 2025 · Abbott Diagnostics Scarborough, Inc. · Class II
• ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model recall
  FDA April 23, 2025 · Abbott Diagnostics Scarborough, Inc. · Class II
• ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model recall
  FDA April 23, 2025 · Abbott Diagnostics Scarborough, Inc. · Class II
• restor3d Cordera Hip System recall
  FDA April 23, 2025 · Conformis Inc. · Class II
• Welch Allyn 2-Piece Reusable Blood Pressure Cuff Kits labeled as: 1… recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Welch Allyn DuraShock Aneroid Gauge Sets with a Reusable Blood Pressure… recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Welch Allyn Green Series 777 Wall System, Product Code/Part Numbers: 1)… recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Welch Allyn Spot Vital Signs 4400 Device, Product Code/Part Numbers: 1)… recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Welch Allyn Connex Vital Signs Monitor, Product Code/Part Numbers: 1) )… recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Welch Allyn Welch Allyn Connex Spot Monitor… recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Welch Allyn Connex Integrated Wall System, Product Code/Part Numbers: 1)… recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• TLX/TLC SP Guided Implant Driver, for ratchet, stainless steel recall
  FDA April 23, 2025 · Straumann USA LLC · Class II
• Welch Allyn CP150 Electrocardiograph recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Welch Allyn CONNEX Accessory Power Management Stand recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Welch Allyn Connex Vital Signs Monitor (CVSM) recall
  FDA April 23, 2025 · Baxter Healthcare Corporation · Class II
• Aveir DR Leadless Pacemaker (LP) Ventricular Device recall
  FDA April 23, 2025 · Abbott Medical · Class II
• Venue Fit Models: R3 (Model Number H45303VFSC, H45303VFSW)… recall
  FDA April 23, 2025 · GE Medical Systems, LLC · Class II
• Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG)… recall
  FDA April 23, 2025 · GE Medical Systems, LLC · Class II
• Philips DXR System, DuraDiagnost Rel recall
  FDA April 23, 2025 · Philips North America Llc · Class II
• Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System recall
  FDA April 23, 2025 · Philips North America Llc · Class II
• MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0… recall
  FDA April 23, 2025 · CareFusion 303, Inc. · Class II
• 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
• 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