Event Notification Report for April 27, 2007
U.S. Nuclear Regulatory Commission
Operations Center
EVENT REPORTS FOR
04/26/2007 - 04/27/2007
Power Reactor
Event Number: 43323
Facility: INDIAN POINT
Region: 1 State: NY
Unit: [2] [3] []
RX Type: [2] W-4-LP,[3] W-4-LP
NRC Notified By: KEITH DROWN
HQ OPS Officer: BILL HUFFMAN
Region: 1 State: NY
Unit: [2] [3] []
RX Type: [2] W-4-LP,[3] W-4-LP
NRC Notified By: KEITH DROWN
HQ OPS Officer: BILL HUFFMAN
Notification Date: 04/27/2007
Notification Time: 17:54 [ET]
Event Date: 04/27/2007
Event Time: 15:44 [EDT]
Last Update Date: 04/27/2007
Notification Time: 17:54 [ET]
Event Date: 04/27/2007
Event Time: 15:44 [EDT]
Last Update Date: 04/27/2007
Emergency Class: NON EMERGENCY
10 CFR Section:
50.72(b)(2)(xi) - OFFSITE NOTIFICATION
10 CFR Section:
50.72(b)(2)(xi) - OFFSITE NOTIFICATION
Person (Organization):
JAMES TRAPP (R1)
JAMES TRAPP (R1)
| Unit | SCRAM Code | RX Crit | Initial PWR | Initial RX Mode | Current PWR | Current RX Mode |
|---|---|---|---|---|---|---|
| 2 | N | Y | 100 | Power Operation | 100 | Power Operation |
| 3 | N | Y | 1 | Startup | 1 | Startup |
INADVERTENT SIREN ACTUATION
"This is a voluntary report under 10 CFR 50.72(b)(2)(xi). Approximately 1544 EST, the new siren system in Westchester County actuated inadvertently during testing. A press release has been issued. There has not been an event related to the health and safety of the public or onsite personnel, or protection of the environment."
The New York Public Utility Commission has been notified. The licensee will notify the NRC Resident Inspector.
"This is a voluntary report under 10 CFR 50.72(b)(2)(xi). Approximately 1544 EST, the new siren system in Westchester County actuated inadvertently during testing. A press release has been issued. There has not been an event related to the health and safety of the public or onsite personnel, or protection of the environment."
The New York Public Utility Commission has been notified. The licensee will notify the NRC Resident Inspector.
General Information or Other
Event Number: 43356
Rep Org: OK DEQ RAD MANAGEMENT
Licensee: ST ANTHONY HOSPITAL
Region: 4
City: OKLAHOMA CITY State: OK
County:
License #: OK-01428-03
Agreement: Y
Docket:
NRC Notified By: MIKE BRODERICK
HQ OPS Officer: MARK ABRAMOVITZ
Licensee: ST ANTHONY HOSPITAL
Region: 4
City: OKLAHOMA CITY State: OK
County:
License #: OK-01428-03
Agreement: Y
Docket:
NRC Notified By: MIKE BRODERICK
HQ OPS Officer: MARK ABRAMOVITZ
Notification Date: 05/11/2007
Notification Time: 10:55 [ET]
Event Date: 04/27/2007
Event Time: 00:00 [CDT]
Last Update Date: 05/14/2007
Notification Time: 10:55 [ET]
Event Date: 04/27/2007
Event Time: 00:00 [CDT]
Last Update Date: 05/14/2007
Emergency Class: NON EMERGENCY
10 CFR Section:
10 CFR Section:
Person (Organization):
VINCENT GADDY (R4)
SCOTT FLANDERS (FSME)
GREG MORELL (FSME)
VINCENT GADDY (R4)
SCOTT FLANDERS (FSME)
GREG MORELL (FSME)
AGREEMENT STATE REPORT MEDICAL EVENT - PATIENT UNDERDOSE
A patient was to receive 150 mCi of I-131 for thyroid cancer on April 27, 2007. The dose was two capsules in a single vial (tube). The intended dose activity was reported to be correct. The patient was presented with the vial containing the dosage. The patient took the dosage. The vial and lead container were placed in storage. On May 9, 2007 a nuclear medical technician discovered a capsule in the vial. The patient had received one-half of the intended dose. The technician reported the discovery to the RSO who reported the incident to the Oklahoma Radiation Management Section supervisor (May 9, 2007 at 5:26 p.m.) by e-mail. Radiation Management Section investigators interviewed St. Anthony Hospital nuclear medicine technicians on May 10, 2007. The patient will be notified. The RSO will submit a written report within 15 days of the initial report. The unused capsule will decay-in-storage.
State of Oklahoma Medical Event reportable under 10CFR35.3045(a)(1)(i)
Event Cause Failure to verify that the entire dose was administered
A "Medical Event" may indicate potential problems in a medical facility's use of radioactive materials. It does not necessarily result in harm to the patient.
* * * UPDATE BY E-MAIL AT 07:01 ON 5/14/2007 FROM C. FLANNERY TO M. ABRAMOVITZ * * *
"This event has been reviewed and determined to be a reportable medical event."
A patient was to receive 150 mCi of I-131 for thyroid cancer on April 27, 2007. The dose was two capsules in a single vial (tube). The intended dose activity was reported to be correct. The patient was presented with the vial containing the dosage. The patient took the dosage. The vial and lead container were placed in storage. On May 9, 2007 a nuclear medical technician discovered a capsule in the vial. The patient had received one-half of the intended dose. The technician reported the discovery to the RSO who reported the incident to the Oklahoma Radiation Management Section supervisor (May 9, 2007 at 5:26 p.m.) by e-mail. Radiation Management Section investigators interviewed St. Anthony Hospital nuclear medicine technicians on May 10, 2007. The patient will be notified. The RSO will submit a written report within 15 days of the initial report. The unused capsule will decay-in-storage.
State of Oklahoma Medical Event reportable under 10CFR35.3045(a)(1)(i)
Event Cause Failure to verify that the entire dose was administered
A "Medical Event" may indicate potential problems in a medical facility's use of radioactive materials. It does not necessarily result in harm to the patient.
* * * UPDATE BY E-MAIL AT 07:01 ON 5/14/2007 FROM C. FLANNERY TO M. ABRAMOVITZ * * *
"This event has been reviewed and determined to be a reportable medical event."