Signals
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.
| Published | Source | Title | Tags |
|---|---|---|---|
| Feb 18, 2026 | FDA device recall | Olympus Corporation of the Americas: Insufflator, Laparoscopic | FDA recall, medical device, class 2, Obstetrics/Gynecology |
| Feb 18, 2026 | FDA device recall | Olympus Corporation of the Americas: Insufflator, Laparoscopic | FDA recall, medical device, class 2, Obstetrics/Gynecology |
| Feb 17, 2026 | FDA device recall | Auris Health, Inc: Bronchoscope (Flexible Or Rigid) | FDA recall, medical device, class 2, Ear, Nose, Throat |
| Feb 17, 2026 | Federal Register | Privacy Act of 1974; System of Records | HIPAA, Notice, Health and Human Services Department, information blocking |
| Feb 13, 2026 | Federal Register | Proposed Information Collection Activity: 2024 Low Income Home Energy Assistance Program (LIHEAP) Residential Energy Consumption Survey (RECS) Data Match | information blocking, Notice, Health and Human Services Department, Children and Families Administration |
| Feb 13, 2026 | Federal Register | Determination of Regulatory Review Period for Purposes of Patent Extension; AMTAGVI | information blocking, Notice, Health and Human Services Department, Food and Drug Administration |
| Feb 13, 2026 | Federal Register | Agency Information Collection Activities: Submission for OMB Review; Comment Request | HIPAA, Notice, Health and Human Services Department, Centers for Medicare & Medicaid Services |
| Feb 12, 2026 | FDA device recall | Intuitive Surgical, Inc.: System, Surgical, Computer Controlled Instrument | FDA recall, medical device, class 2, Gastroenterology, Urology |
| Feb 11, 2026 | Federal Register | Patient Protection and Affordable Care Act, HHS Notice of Benefit and Payment Parameters for 2027; and Basic Health Program | HIPAA, Proposed Rule, Health and Human Services Department, Centers for Medicare & Medicaid Services |
| Feb 3, 2026 | FDA device recall | Focalyx Technologies, LLC.: System, Image Processing, Radiological | FDA recall, medical device, class 2, Radiology |
| Feb 3, 2026 | FDA device recall | Siemens Medical Solutions USA, Inc: System, X-Ray, Tomography, Computed | FDA recall, medical device, class 2, Radiology |
| Feb 3, 2026 | FDA device recall | Siemens Medical Solutions USA, Inc: System, X-Ray, Tomography, Computed | FDA recall, medical device, class 2, Radiology |
| Feb 3, 2026 | FDA device recall | Siemens Medical Solutions USA, Inc: System, X-Ray, Tomography, Computed | FDA recall, medical device, class 2, Radiology |
| Feb 3, 2026 | FDA device recall | Siemens Medical Solutions USA, Inc: System, X-Ray, Tomography, Computed | FDA recall, medical device, class 2, Radiology |
| Feb 2, 2026 | FDA device recall | Medtronic MiniMed, Inc.: Automated Insulin Dosing Device System, Single Hormonal Control | FDA recall, medical device, class 3, Unknown |
| Feb 2, 2026 | FDA device recall | Beckman Coulter, Inc.: Automated Pipetting, Diluting And Specimen Processing Workstations For Flow Cytometric Analysis | FDA recall, medical device, class 1, Clinical Chemistry |
| Feb 2, 2026 | FDA device recall | Intuitive Surgical, Inc.: System, Surgical, Computer Controlled Instrument | FDA recall, medical device, class 2, Gastroenterology, Urology |
| Jan 29, 2026 | FDA device recall | CareFusion 303, Inc.: Pump, Infusion | FDA recall, medical device, class 2, General Hospital |
| Jan 28, 2026 | Federal Register | Annual Civil Monetary Penalties Inflation Adjustment | HIPAA, Rule, Health and Human Services Department, information blocking |
| Jan 26, 2026 | Federal Register | National Vaccine Injury Compensation Program; List of Petitions Received | information blocking, Notice, Health and Human Services Department, Health Resources and Services Administration |
| Jan 23, 2026 | Federal Register | Proposed Information Collection Activity; Procedures for Requests From Tribal Lead Agencies To Use Child Care and Development Funds for Construction or Major Renovation of Child Care Facilities | information blocking, Notice, Health and Human Services Department, Children and Families Administration |
| Jan 23, 2026 | Federal Register | Tyler Jordan Hall: Final Debarment Order | information blocking, Notice, Health and Human Services Department, Food and Drug Administration |
| Jan 22, 2026 | FDA device recall | Philips North America: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Oximeter | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Oximeter | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: System, Monitoring, Perinatal | FDA recall, medical device, class 2, Obstetrics/Gynecology |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Oximeter | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: Oximeter | FDA recall, medical device, class 2, Cardiovascular |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: System, Monitoring, Perinatal | FDA recall, medical device, class 2, Obstetrics/Gynecology |
| Jan 22, 2026 | FDA device recall | Edan Diagnostics: System, Monitoring, Perinatal | FDA recall, medical device, class 2, Obstetrics/Gynecology |
| Jan 16, 2026 | FDA device recall | Mazor Robotics Ltd: Orthopedic Stereotaxic Instrument | FDA recall, medical device, class 2, Neurology |
| Jan 16, 2026 | FDA device recall | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Interventional Fluoroscopic X-Ray System | FDA recall, medical device, class 2, Radiology |
| Jan 14, 2026 | FDA device recall | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Interventional Fluoroscopic X-Ray System | FDA recall, medical device, class 2, Radiology |
| Jan 14, 2026 | FDA device recall | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Interventional Fluoroscopic X-Ray System | FDA recall, medical device, class 2, Radiology |
| Jan 14, 2026 | Federal Register | Tribal Consultation on Proposed Modifications to the HIPAA Privacy Rule | HIPAA, Proposed Rule, Health and Human Services Department |
| Jan 13, 2026 | Federal Register | Agency Information Collection Request; 30-Day Public Comment Request | HIPAA, Notice, Health and Human Services Department, cybersecurity |
| Jan 12, 2026 | NIST news | CAISI Issues Request for Information About Securing AI Agent Systems | NIST |
| Jan 8, 2026 | FDA device recall | Securitas Healthcare LLC: System, Environmental Control, Powered | FDA recall, medical device, class 2, Physical Medicine |
| Jan 8, 2026 | FDA device recall | Securitas Healthcare LLC: System, Environmental Control, Powered | FDA recall, medical device, class 2, Physical Medicine |
| Jan 8, 2026 | FDA device recall | CareFusion 303, Inc.: Cabinet, Table And Tray, Anesthesia | FDA recall, medical device, class 1, Anesthesiology |
| Jan 8, 2026 | FDA device recall | Siemens Medical Solutions USA, Inc: Interventional Fluoroscopic X-Ray System | FDA recall, medical device, class 2, Radiology |