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EA-04-215 - The Milton S. Hershey Medical CenterOctober 14, 2005 EA-04-215 L. K. Thompson
Dear Mr. Thompson: In a letter dated May 18, 2005, the NRC provided you with the results of four investigations conducted by the NRC Office of Investigations (OI), Region I Field Office, between May 11, 2004 and March 16, 2005, to determine whether licensed byproduct material was improperly used by employees of the Milton S. Hershey Medical Center (MSHMC). Our letter noted, in part, that based on the evidence developed during these investigations, OI concluded that (1) in the 1996 - 1997 time frame, an authorized user deliberately administered byproduct material to an individual, with no medical reason, for the sole purpose of comparing images from two cameras, (2) in 2002, a former MSHMC employee deliberately used byproduct material to perform an unauthorized bone scan on himself, (3) in 2004, a MSHMC employee deliberately used byproduct material to perform an unauthorized brain scan on herself, and (4) an unauthorized nuclear medicine scan of a worker’s lower extremities in the early 1990s could not be substantiated. In addition, our letter informed you that after further review of all the available evidence regarding the first investigation noted above, the NRC staff concluded that the authorized user’s administration of byproduct material to perform a comparison of images from two cameras violated NRC requirements, but that deliberateness was not substantiated. A Factual Summary of the OI investigations was enclosed with our May 18, 2005 letter. In our letter dated May 18, 2005, we informed you that as a result of these OI investigations, two apparent violations were identified and were being considered for escalated enforcement action in accordance with the NRC Enforcement Policy. The first apparent violation involved an authorized user administering byproduct material with no medical reason, contrary to 10 CFR 35.11. The second apparent violation involved the deliberate use of byproduct material by the staff of the MSHMC to perform unauthorized nuclear medicine tests, without the supervision of an authorized user, on two separate occasions, contrary to 10 CFR 35.27(a). As a result of these findings, we understand that the MSHMC took several actions to ensure that these events do not recur. These actions included (1) immediately conducting training with each nuclear medicine technician emphasizing the proper procedure for administering licensed material and the need to obtain authorization from a physician or an Authorized User (AU) prior to each administration, (2) reviewing this event with appropriate MSHMC staff members, and (3) modifying training procedures to include review of this event in new student training and required periodic retraining of current employees. In addition, our letter offered you a choice to (1) attend a Predecisional Enforcement Conference, or (2) request Alternative Dispute Resolution (ADR) with the NRC in an attempt to resolve any disagreement on whether a violation occurred, the appropriate enforcement action, and the appropriate corrective actions. ADR is a general term encompassing various techniques for resolving conflict outside of court using a neutral third party, and the NRC currently has a pilot program for using ADR. The technique that the NRC decided to employ during the pilot program, which is now in effect, is mediation. At your request, an ADR mediation session was held between the MSHMC and the NRC in King of Prussia, PA, on August 23, 2005, and a settlement agreement was reached regarding this matter. The elements of the settlement agreement are as follows:
Enclosed with this letter is the Notice of Violation (Notice) and the Confirmatory Order (Order). By letter dated October 5, 2005, the MSHMC consented to issuance of the Notice of Violation and Confirmatory Order and waived the right to request a hearing on all or any part of the Confirmatory Order. You are not required to respond to this letter or Notice. However, in accordance with the settlement agreement, you are required to respond to the Order. Your written response to the Order, and your response to the Notice, if you choose to provide one, should be sent to the U.S. Nuclear Regulatory Commission, ATTN: Regional Administrator, Region I, 475 Allendale Road, King of Prussia, PA 19406, and marked "Open by Addressee Only", within 30 days of the date of this letter. A copy of this letter and its enclosures will be made available electronically for public inspection in the NRC Public Document Room or from the NRC’s document system (ADAMS). ADAMS is accessible from the NRC Web site at http://www.nrc.gov/reading-rm/adams.html. The NRC will also include this letter on its website for a period of 1 year at www.nrc.gov; select What We Do, Enforcement, Significant Enforcement Actions. In addition, a press release announcing this enforcement action will be issued by the NRC. Your response, if you choose to provide one, will also be made available electronically for public inspection in the NRC Public Document Room or from the NRC’s document system (ADAMS). If you have any questions or comments concerning this letter, please contact Mr. Karl Farrar of my staff at 610-337-5301.
Docket No. 03003203 Enclosures: As Stated
During four separate investigations conducted at the Milton S. Hershey Medical Center (MSHMC) by the NRC Office of Investigations between May 11, 2004, and March 16, 2005, a violation of NRC requirements was identified. In accordance with the NRC Enforcement Policy, the violation is listed below: 10 CFR 35.27(a), requires, in part, that a licensee that permits the receipt, possession, use, or transfer of byproduct material by an individual under the supervision of an authorized user as allowed by 10 CFR 35.11(b)(1), shall require the supervised individual to follow the instructions of the supervising authorized user for medical uses of byproduct material, written radiation protection procedures established by the licensee, written directive procedures, written regulations, and license conditions with respect to the medical use of byproduct material. Contrary to the above, on three separate occasions, licensee individuals used byproduct material to perform unauthorized nuclear medicine tests without the supervision of an authorized user. Specifically:
The NRC has concluded that information regarding the reason for the violation, the corrective actions taken and planned to correct the violation and prevent recurrence, and the date when full compliance will be achieved is already adequately addressed on the docket in the letter forwarding this Notice. However, you are required to submit a written statement or explanation pursuant to 10 CFR 2.201 if the description herein does not accurately reflect your corrective actions or your position. In that case, or if you choose to respond, your written response should be sent to the U.S. Nuclear Regulatory Commission, ATTN: Regional Administrator, Region I, 475 Allendale Road, King of Prussia, PA 19406, and marked "Open by Addressee Only" within 30 days of the date of the letter transmitting this Notice. This reply should be clearly marked as a "Reply to a Notice of Violation, EA-04-215." Because your response will be made available electronically for public inspection in the NRC Public Document Room or from the NRC’s document system (ADAMS), accessible from the NRC Web site at http://www.nrc.gov/reading-rm/adams.html, to the extent possible, it should not include any personal privacy, proprietary, or safeguards information so that it can be made available to the public without redaction. If personal privacy or proprietary information is necessary to provide an acceptable response, then please provide a bracketed copy of your response that identifies the information that should be protected and a redacted copy of your response that deletes such information. If you request withholding of such material, you must specifically identify the portions of your response that you seek to have withheld and provide in detail the bases for your claim of withholding (e.g., explain why the disclosure of information will create an unwarranted invasion of personal privacy or provide the information required by 10 CFR 2.390(b) to support a request for withholding confidential commercial or financial information). If safeguards information is necessary to provide an acceptable response, please provide the level of protection described in 10 CFR 73.21. In accordance with 10 CFR 19.11, you may be required to post this Notice within two working days. Dated this 14th day of October 2005.
CONFIRMATORY ORDER The Milton S. Hershey Medical Center (MSHMC) is the holder of Byproduct Material License 37-13831-01 issued by the Nuclear Regulatory Commission (NRC or Commission) pursuant to 10 CFR Parts 30 and 35. This broad scope medical license authorizes possession and use of a wide variety of radionuclides for medical diagnosis, therapy, and research in humans; research and development as defined in 10 CFR 30.4, including animal studies; instrument calibration; student instruction; and in vitro studies. The license further authorizes possession and use of iridium-192 sealed sources for medical use permitted by 10 CFR 35.600 in a high dose rate remote afterloader, depleted uranium for shielding in a linear accelerator, and barium-133 sealed sources for use in a device for patient attenuation correction during S.P.E.C.T. imaging. The license, originally issued on October 16, 1970, was renewed on August 4, 1995, and is currently under timely renewal. II In a letter dated May 18, 2005, the NRC provided MSHMC with the results of four investigations conducted by the NRC Office of Investigations (OI), Region I Field Office, between May 11, 2004 and March 16, 2005, to determine whether licensed byproduct material was improperly used by its employees. This letter stated that, based on the evidence developed during these investigations, the NRC concluded that (1) in the 1996 - 1997 time frame, the authorized user’s administration of byproduct material to perform a comparison of images from two cameras violated NRC requirements, but that deliberateness was not substantiated, (2) in 2002, a former MSHMC employee deliberately used byproduct material to perform an unauthorized bone scan on himself, (3) in 2004, a MSHMC employee deliberately used byproduct material to perform an unauthorized brain scan on herself, and (4) an unauthorized nuclear medicine scan of a worker’s lower extremities in the early 1990s could not be substantiated. III In response to the NRC’s May 18, 2005, letter, MSHMC immediately took several actions to ensure that these events do not recur. These actions included: (1) conducting training with each nuclear medicine technician emphasizing the proper procedure for administering licensed material and the need to obtain authorization from a physician or an Authorized User (AU) prior to each administration; (2) reviewing this event with appropriate MSHMC staff members; and (3) modifying training procedures to include review of this event in new student training and required periodic retraining of current employees. MSHMC also requested the use of Alternative Dispute Resolution (ADR) to bring closure to this matter. The NRC uses ADR, a process in which a neutral mediator, with no decision-making authority, assists the NRC and a regulated party (in this case, MSHMC), to resolve disagreements as to whether a violation has occurred, the appropriate enforcement action to be taken, and the appropriate corrective actions to be taken. An ADR session was held between the NRC and MSHMC in Region I, King of Prussia, PA, on August 23, 2005. The ADR session was mediated by a professional mediator, arranged through Cornell University’s Institute of Conflict Management. During that ADR session, a settlement agreement was reached. The elements of the settlement agreement consist of the following:
By letter dated October 5, 2005, the MSHMC consented to issuance of the Notice of Violation and this Confirmatory Order with the commitments, as described in Section IV. The MSHMC further agreed in its October 5, 2005, letter that this Order is to be effective upon issuance and that it has waived its right to a hearing. I find that the MSHMC’s commitments as set forth in Section IV are acceptable and necessary, and that the NRC’s concerns can be resolved by confirming the MSHMC’s commitments as outlined in this Confirmatory Order. I conclude that with these commitments the public health and safety are reasonably assured. In view of the foregoing, I have determined that the public health and safety require that the Licensee’s commitments be confirmed by this Order. Based on the above and the MSHMC’s consent, this Confirmatory Order is immediately effective upon issuance. IV Accordingly, pursuant to Sections 81, 161b, 161i, 161o, 182, and 186 of the Atomic Energy Act of 1954, as amended, and the Commission's regulations in 10 CFR § 2.202 and 10 CFR Parts 30 and 35, IT IS HEREBY ORDERED, THAT BY AUGUST 23, 2006:
The Director, Office of Enforcement, may relax or rescind, in writing, any of the above conditions upon a showing by MSHMC of good cause. V Any person adversely affected by this Confirmatory Order, other than the MSHMC, may request a hearing within 20 days of its issuance. Where good cause is shown, consideration will be given to extending the time to request a hearing. A request for extension of time must be made in writing to the Director, Office of Enforcement, U.S. Nuclear Regulatory Commission, Washington, D.C. 20555, and must include a statement of good cause for the extension. Any request for a hearing shall be submitted to the Secretary, U.S. Nuclear Regulatory Commission, ATTN: Chief, Rulemaking and Adjudications Staff, Washington, D.C. 20555. Copies of the hearing request shall also be sent to the Director, Office of Enforcement, U.S. Nuclear Regulatory Commission, Washington, D.C. 20555, to the Assistant General Counsel for Materials Litigation and Enforcement, to the Director of the Division of Regulatory Improvement Programs at the same address, and to MSHMC. Because of continuing disruptions in delivery of mail to United States Government offices, it is requested that answers and requests for hearing be transmitted to the Secretary of the Commission either by means of facsimile transmission to 301-415-1101 or by e-mail to hearingdocket@nrc.gov and also to the Office of the General Counsel by means of facsimile transmission to 301-415-3725 or e-mail to OGCMailCenter@nrc.gov. If such a person requests a hearing, that person shall set forth with particularity the manner in which his interest is adversely affected by this Order and shall address the criteria set forth in 10 CFR § 2.309 (d) and (f). If a hearing is requested by a person whose interest is adversely affected, the Commission will issue an Order designating the time and place of any hearing. If a hearing is held, the issue to be considered at such hearing shall be whether this Confirmatory Order shall be sustained. In the absence of any request for hearing, or written approval of an extension of time in which to request a hearing, the provisions specified in Section V above shall be final 20 days from the date of this Order without further order or proceedings. If an extension of time for requesting a hearing has been approved, the provisions specified in Section V shall be final when the extension expires if a hearing request has not been received. AN ANSWER OR A REQUEST FOR A HEARING SHALL NOT STAY THE IMMEDIATE EFFECTIVENESS OF THIS ORDER.
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