-
Quantum Informatics - VIPER Product Name: Monitor, Physiological… recall
FDA
· Spectrum Medical Ltd. · Class II
-
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP… recall
FDA
· Remote Diagnostic Technologies Ltd. · Class II
-
Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090… recall
FDA
· Radiometer Medical ApS · Class II
-
BD PYXIS MEDBANK (Name recall
FDA
· CareFusion 303, Inc. · Class II
-
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 recall
FDA
· Medtronic Xomed, Inc. · Class II
-
Tandem Mobi Insulin Pump with Interoperable Technology recall
FDA
· Tandem Diabetes Care, Inc. · Class I
-
t:slim X2 Insulin Pump with Interoperable Technology recall
FDA
· Tandem Diabetes Care, Inc. · Class I
-
Atellica CH Revised C Reactive Protein (RCRP) recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID BD… recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex… recall
FDA
· CareFusion 303, Inc. · Class II
-
Stimulation RC Clinician Programmer Application, Model A71400… recall
FDA
· Medtronic Neuromodulation · Class II
-
stryker HoloBlueprint Application recall
FDA
· Tornier S.A.S. · Class II
-
stryker Blueprint Mixed Reality Instrument Kit recall
FDA
· Tornier S.A.S. · Class II
-
stryker Blueprint Mixed Reality Depth Stop Pin recall
FDA
· Tornier S.A.S. · Class II
-
stryker Blueprint Mixed Reality Glenoid Box Lid recall
FDA
· Tornier S.A.S. · Class II
-
stryker Blueprint Mixed Reality Box Base recall
FDA
· Tornier S.A.S. · Class II
-
stryker Blueprint Mixed Reality Instrument Check Block recall
FDA
· Tornier S.A.S. · Class II
-
stryker Blueprint Mixed Reality Coracoid Clamp recall
FDA
· Tornier S.A.S. · Class II
-
stryker Blueprint Mixed Reality Glenoid Digitizer recall
FDA
· Tornier S.A.S. · Class II
-
stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless… recall
FDA
· Tornier S.A.S. · Class II
-
DxC 500 AU Clinical Chemistry Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
Baxter TruSystem 7500, Product Code 4091000 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid Plus (SC), Product Code 1854088 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Floor mounting column TS 7500 U, Product Code 1730732 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Stationary column TruSystem 7500 U, Product Code 1730731 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Mobile column TruSystem 7500 U, Product Code 1730720 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Mobile column TruSystem 7500, Product Code 1717023 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Floor mounting column TruSystem 7500, Product Code 1717021 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Stationary column TruSystem 7500, Product Code 1717020 recall
FDA
· Baxter Healthcare Corporation · Class II
-
Baxter Operating table column TS7500 MOBIUS, Product Code 1704695 recall
FDA
· Baxter Healthcare Corporation · Class II
-
BD Pyxis: Anesthesia Station ES recall
FDA
· CareFusion 303, Inc. · Class II
-
Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
BD Care Coordination Engine (CCE) Infusion Adapter… recall
FDA
· CareFusion 303, Inc. · Class I
-
BD Alaris Systems Manager recall
FDA
· CareFusion 303, Inc. · Class I
-
MIM software recall
FDA
· MIM Software Inc · Class II
-
Philips IntelliSpace Cardiovascular software, Model 830089 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Leica Biosystems Cryostats Product Name: CM1950 Model recall
FDA
· Leica Biosystems Nussloch Gmbh · Class II
-
DxC 500 AU Clinical Chemistry Analyzer recall
FDA
· Beckman Coulter Laboratory Systems (Suzhou) CO., Ltd. · Class II
-
IntelePACS (Image Fusion Module) - InteleViewer recall
FDA
· Intelerad Medical Systems Incorporated · Class II
-
MOSAIQ Oncology Information System recall
FDA
· Elekta, Inc. · Class II
-
(1) Pyxis MedStation ES recall
FDA
· CareFusion 303, Inc. · Class II
-
UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number… recall
FDA
· Medicrea International · Class II
-
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137 recall
FDA
· Beckman Coulter, Inc. · Class II
-
Ivenix Infusion System (IIS), LVP Software LVP-SW-0005… recall
FDA
· Fresenius Kabi USA, LLC · Class I
-
VITROS Product Name: VITROS 3600 Immunodiagnostic System Model recall
FDA
· Ortho-Clinical Diagnostics, Inc. · Class II
-
VITROS Product Name: VITROS XT 7600 Integrated System Model recall
FDA
· Ortho-Clinical Diagnostics, Inc. · Class II
-
VITROS Product Name: VITROS 5600 Integrated System Model recall
FDA
· Ortho-Clinical Diagnostics, Inc. · Class II
-
Change Healthcare Cardiology Hemodynamics software recall
FDA
· A L I Technologies Ltd · Class II
-
Change Healthcare Cardiology Hemo software recall
FDA
· A L I Technologies Ltd · Class II
-
McKesson Cardiology Hemo software recall
FDA
· A L I Technologies Ltd · Class II
-
Portrait Core Services, a set of software services that enable the… recall
FDA
· GE Medical Systems, LLC · Class II
-
BD Pyxis MedStation ES (Med ES Main) recall
FDA
· CareFusion 303, Inc. · Class II
-
Xhibit Telemetry Receiver with Software, Model 96280… recall
FDA
· Spacelabs Healthcare, Inc. · Class II
-
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps… recall
FDA
· Medtronic Neuromodulation · Class II
-
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps… recall
FDA
· Medtronic Neuromodulation · Class II