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Information Notices of Interest to Medical Use Licensees

The following notices are listed by year:

2000s: 2021 2019 2017 2016 2014 2013 2012 2011
2010 2009 2008 2007 2006 2005 2004 2003
2002 2001 2000
1900s: 1999 1998 1986

 

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2021
IN-2021-02 08/04/2021 Recent Issues Associated with Monitoring Occupational Exposure to Radiation from Licensed and Unlicensed Radiation Sources
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2019
IN-2019-12 12/31/2019 Recent Reported Medical Events Involving the Administration of Yttrium-90 Microspheres for Therapeutic Medical Procedures
IN-2019-11 12/23/2019 Strontium-82/Rubidium-82 Generator Elution Events and Issues
IN-2019-07 08/26/2019 Methods to prevent medical events
IN-2019-06 08/26/2019 Patient skin contamination events Associated with I-131 Metaiodobenzylguanidine during Neuroblastoma treatments
IN-2019-04 08/14/2019 Effective Cyber Security Practices to Protect Digital Assets of Byproduct Materials Licensees
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2017
IN-2017-02 05/17/2017 Best Practice Concepts for Patient Release
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2016
IN-2016-03 01/12/2016 Revision to the National Institute of Standards and Technology Standard for Radium-223 and Impact on Dose Calibration for the Medical Use of Radium-223 Dichloride
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2014
IN-2014-05 05/12/2014 Verifying Appropriate Dosimetry Evaluation
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2013
IN-2013-16 08/12/2013 Importance of Verification of Treatment Parameters for High Dose-Rate Remote Afterloader Administrations
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2012
IN-2012-08 04/10/2012 High Dose-Rate Remote Afterloader (HDR) Physical Presence Requirements
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2011
IN-2011-11 04/27/2011 Reporting Requirement For Heat And Smoke Detector Failures In 10 CFR Part 36 Irradiators
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2010
IN-2010-24 11/19/2010 Notice of Possible Source Leakage During Non-Routine Maintenance on a Gammacell 40 Irradiator
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2009
IN-2009-30 11/06/2009 Findings From The NRC Initiative To Assess Materials Licensees' Compliance With The NRC Decommissioning Requirements
IN-2009-27 11/13/2009 Revised International Nuclear And Radiological Event Scale User's Manual
IN-2009-17 08/28/2009 Reportable Medical Events Involving Treatment Delivery Errors Caused By Confusion Of Units For The Specification Of Brachytherapy Sources
IN-2009-15 08/28/2009 Varian Medical Systems Varisource High Dose-Rate Remote Afterloader Events: Source Retraction Problems
IN-2009-07 03/30/2009 Withholding of Propriety Information from Public Disclosure
IN-2009-05 02/03/2009 Contamination Events Resulting From Damage To Sealed Radioactive Sources During Gauge Dismantlement And Non-Routine Maintenance Operations
IN-2009-01 01/22/2009 National Response Framework
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2008
IN-2008-22 01/12/2009 Molybdenum-90 Breakthrough in Molybdenum-99/Technetium-99m Generators
IN-2008-03 05/16/2008 Precautions to take before Sharing Sensitive Security-Related Information
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2007
IN-2007-38 12/14/2007 Ensuring Complete and Accurate Information in the Documentation of Training and Experience for Individuals Seeking Approval as Medical Authorized Users
IN-2007-35 10/17/2007 Varian Medical Systems Varisource HDR Events: Iridium-192 Source Pulled From Shielded Position
IN-2007-25 07/19/2007 Suggestion from the Advisory Committee on the Medical Use of Isotopes for Consideration to Improve Compliance With Sodium Iodide I-131 Written Directive Requirements in 10 CFR 35.40 and Supervision Requirements in 10 CFR 35.27
IN-2007-16 05/02/2007 Common Violations of the Increased Controls Requirements and Related Guidance Documents
IN-2007-10 03/05/2007 Yttrium-90 Therashperes and SIRSpheres Impurities
IN-2007-08 02/28/2007 Potential vulnerabilities of time-reliant computer-based systems due to change in daylight saving time dates
IN-2007-03 02/02/2007 Reportable Medical Events Involving Patients Receiving Dosages of Sodium Iodide Iodine-131 Less Than the Prescribed Dosage Because of Capsules Remaining in Vials After Administration
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2006
IN-2006-12 07/06/2006 Exercising Due Diligence when Transferring Radioactive Materials
IN-2006-11 06/12/2006 Applicability of Patient Intervention in Determining Medical Events for Gamma Stereotactic Radiosurgery and Other Therapy Procedures
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2005
IN-2005-27 10/07/2005 Low-Dose-Rate Manual Brachytherapy – Equipment-Related Medical Events
IN-2005-17 06/23/2005 Manual Brachytherapy Source Jamming
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2004
IN-2004-02 02/05/2004 Strontium-90 Eye Applicators: New Calibration Values and Use
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2003
IN-2003-22 12/09/2003 Heightened Awareness for Patients Containing Detectable Amounts of Radiation from Medical Administrations
IN-2003-21 11/24/2003 High-Dose-Rate-Remote-Afterloader Equipment Failure
IN-2003-12 08/22/2003 Problems Involved in Monitoring Dose to the Hands Resulting from the Handling of Radiopharmaceuticals
IN-2003-09 07/16/2003 Source Positioning Errors and System Malfunctions During Administration of Intravascular Brachytherapy
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2002
IN-2002-36 12/27/2002 Incomplete of Inaccurate Information Provided to the Licensee And/or NRC by Any Contractor or Subcontractor Employee
IN-2002-33 11/22/2002 Notification of Permanent Injunction Against Neutron Products Incorporated of Dickerson, Maryland
IN-2002-28 09/27/2002 Appointment of Radiation Safety Officers and Authorized Users Under 10 CFR Part 35
IN-2002-23 07/16/2002 Unauthorized Administration of Byproduct Material for Medical Use
IN-2002-23s1 03/21/2003 Unauthorized Administration of Byproduct Material for Medical Use
IN-2002-19 06/14/2002 Medical Misadministrations Caused by Failure to Properly Perform Tests on Dose Calibrators for Beta -and Low-Energy Photon-Emitting Radionuclides
IN-2002-17 05/30/2002 Medical Use of Strontium-90 Eye Applicators: New Requirements for Calibration and Decay Correction
IN-2002-16 05/01/2002 Intravascular Brachytherapy Misadministrations
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2001
IN-2001-08s1 06/06/2001 Update on the Investigation of Patient Deaths in Panama, Following Radiation Therapy Overexposures
IN-2001-08 06/01/2001 Treatment Planning System Errors Result in Deaths of Overseas Radiation Therapy Patients
IN-2001-01 03/26/2001 The Importance of Accurate Inventory Controls to Prevent the Unauthorized Possession of Radioactive Material
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2000
IN-2000-22 12/18/2000 Medical Misadministrations Caused by Human Errors Involving Gamma Stereotactic Radiosurgery (Gamma Knife)
IN-2000-19 12/05/2000 Implementation of Human Use Research Protocols Involving U.S. Nuclear Regulatory Commission Regulated Materials
IN-2000-16 10/05/2000 Potential Hazards Due to Volatilization of Radionuclides
IN-2000-10 07/18/2000 Recent Events Resulting in Extremity Exposures Exceeding Regulatory Limits
IN-2000-05 03/06/2000 Recent Medical Misadministrations Resulting from Inattention to Detail
IN-2000-04 02/25/2000 Enforcement Sanctions for Deliberate Violations of NRC Employee Protection Requirements
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1999
IN-99-27 09/02/1999 Malfunction of Source Retraction Mechanism in Cobalt-60 Teletherapy Treatment Units
IN-99-23 7/06/1999 Safety Concerns Related to Repeated Control Unit Failures of the Nucletron Classic Model High-Dose-Rate Remote Afterloading Brachytherapy Devices
IN-99-11 4/16/1999 Incidents Involving the Use of Radioactive Iodine-131
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1998
IN-98-12 4/03/1998 Licensees' Responsibilities Regarding Reporting and Follow-Up Requirements for Nuclear-Powered Pacemakers
IN-98-10 3/09/1998 Probable Misadministrations Occurring During Intravascular Brachytherapy with the Novoste Beta-Cath System
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1986
IN-86-59 07/14/1986 Increased Monitoring of Certain Patients with Implanted Coratomic, Inc, Model C-100 and C-101 Nuclear-Powered Cardiac Pacemakers
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Page Last Reviewed/Updated Thursday, March 24, 2022