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Regulatory notices, standards drafts, advisories and device recalls that matter to healthcare security, refreshed every six hours from the publishing agencies. Breach reports have their own register. Where each item comes from, and how fresh it is: sources.

Showing items from openFDA device recalls (U.S. Food and Drug Administration). About this sourceShow all sources
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211 signals, showing 1 to 50Page 1 of 5Next
PublishedSourceTitleTags
Sep 18, 2026FDA device recallPhilips Ultrasound, LLC: System, Imaging, Pulsed Doppler, UltrasonicFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 18, 2026FDA device recallPhilips North America Llc: System, Nuclear Magnetic Resonance ImagingFDA recall, medical device, class 2, Radiology
Sep 15, 2026FDA device recallPTW FREIBURG: Accelerator, Linear, MedicalFDA recall, medical device, class 2, Radiology
Sep 14, 2026FDA device recallNuclein LLC: Instrumentation For Clinical Multiplex Test SystemsFDA recall, medical device, class 2, Clinical Chemistry
Sep 11, 2026FDA device recallPhilips North America: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)FDA recall, medical device, class 2, Cardiovascular
Sep 11, 2026FDA device recallPhilips North America: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)FDA recall, medical device, class 2, Cardiovascular
Sep 11, 2026FDA device recallNova Biomedical Corporation: Prescription Use Blood Glucose Meter For Near-Patient TestingFDA recall, medical device, class 2, Clinical Chemistry
Sep 11, 2026FDA device recallNova Biomedical Corporation: Prescription Use Blood Glucose Meter For Near-Patient TestingFDA recall, medical device, class 2, Clinical Chemistry
Sep 11, 2026FDA device recallNova Biomedical Corporation: Prescription Use Blood Glucose Meter For Near-Patient TestingFDA recall, medical device, class 2, Clinical Chemistry
Sep 11, 2026FDA device recallNova Biomedical Corporation: Prescription Use Blood Glucose Meter For Near-Patient TestingFDA recall, medical device, class 2, Clinical Chemistry
Sep 11, 2026FDA device recallNova Biomedical Corporation: Prescription Use Blood Glucose Meter For Near-Patient TestingFDA recall, medical device, class 2, Clinical Chemistry
Sep 2, 2026FDA device recallMedos International Sarl: Orthopedic Stereotaxic InstrumentFDA recall, medical device, class 2, Neurology
Sep 2, 2026FDA device recallBoston Scientific Corporation: Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)FDA recall, medical device, class 2, Cardiovascular
Sep 2, 2026FDA device recallBoston Scientific Corporation: Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)FDA recall, medical device, class 2, Cardiovascular
Sep 2, 2026FDA device recallBoston Scientific Corporation: Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)FDA recall, medical device, class 2, Cardiovascular
Aug 31, 2026FDA device recallBaxter Healthcare Corporation: Pump, InfusionFDA recall, medical device, class 2, General Hospital
Aug 31, 2026FDA device recallBaxter Healthcare Corporation: Pump, InfusionFDA recall, medical device, class 2, General Hospital
Aug 27, 2026FDA device recallGE Medical Systems Information Technologies Inc: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)FDA recall, medical device, class 2, Cardiovascular
Aug 27, 2026FDA device recallGE Medical Systems Information Technologies Inc: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)FDA recall, medical device, class 2, Cardiovascular
Aug 27, 2026FDA device recallGE Medical Systems Information Technologies Inc: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)FDA recall, medical device, class 2, Cardiovascular
Aug 27, 2026FDA device recallGE Medical Systems Information Technologies Inc: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)FDA recall, medical device, class 2, Cardiovascular
Aug 26, 2026FDA device recallFUJIFILM Healthcare Americas Corporation: System, Image Processing, RadiologicalFDA recall, medical device, class 2, Radiology
Aug 21, 2026FDA device recallMerge Healthcare, Inc.: System, Image Processing, RadiologicalFDA recall, medical device, class 2, Radiology
Aug 17, 2026FDA device recallBeckman Coulter Inc.: Analyzer, Chemistry (Photometric, Discrete), For Clinical UseFDA recall, medical device, class 1, Clinical Chemistry
Aug 17, 2026FDA device recallBeckman Coulter Inc.: Analyzer, Chemistry (Photometric, Discrete), For Clinical UseFDA recall, medical device, class 1, Clinical Chemistry
Aug 14, 2026FDA device recallParagonix Technologies Inc.: System, Perfusion, KidneyFDA recall, medical device, class 2, Gastroenterology, Urology
Aug 14, 2026FDA device recallFoundation Medicine, Inc.: Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection SystemFDA recall, medical device, class 3, Unknown
Aug 10, 2026FDA device recallPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Interventional Fluoroscopic X-Ray SystemFDA recall, medical device, class 2, Radiology
Aug 10, 2026FDA device recallPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Interventional Fluoroscopic X-Ray SystemFDA recall, medical device, class 2, Radiology
Aug 10, 2026FDA device recallPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Interventional Fluoroscopic X-Ray SystemFDA recall, medical device, class 2, Radiology
Aug 4, 2026FDA device recallGE Medical Systems Information Technologies Inc: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)FDA recall, medical device, class 2, Cardiovascular
Aug 4, 2026FDA device recallGE Medical Systems Information Technologies Inc: ElectrocardiographFDA recall, medical device, class 2, Cardiovascular
Aug 3, 2026FDA device recallNuclein LLC: Instrumentation For Clinical Multiplex Test SystemsFDA recall, medical device, class 2, Clinical Chemistry
Jul 31, 2026FDA device recallMUNEVO GMBH: Components, WheelchairFDA recall, medical device, class 1, Physical Medicine
Jul 31, 2026FDA device recallCopan WASP: Calculator/Data Processing Module, For Clinical UseFDA recall, medical device, class 1, Clinical Chemistry
Jul 31, 2026FDA device recallBeckman Coulter Biomedical GmbH: Calculator/Data Processing Module, For Clinical UseFDA recall, medical device, class 1, Clinical Chemistry
Jul 24, 2026FDA device recallPermobil Inc: Wheelchair, PoweredFDA recall, medical device, class 2, Physical Medicine
Jul 24, 2026FDA device recallPermobil Inc: Wheelchair, PoweredFDA recall, medical device, class 2, Physical Medicine
Jul 23, 2026FDA device recallAlphatec Spine, Inc.: Stimulator, Electrical, Evoked ResponseFDA recall, medical device, class 2, Neurology
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