Event Notification Report for April 18, 2025
U.S. Nuclear Regulatory Commission
Operations Center
EVENT REPORTS FOR
04/17/2025 - 04/18/2025
Non-Agreement State
Event Number: 57657
Rep Org: Curium Pharma
Licensee: Curium Pharma
Region: 3
City: Noblesville State: IN
County: Hamilton
License #: 13-35179-02
Agreement: N
Docket:
NRC Notified By: Matthew Trusner
HQ OPS Officer: Tenisha Meadows
Licensee: Curium Pharma
Region: 3
City: Noblesville State: IN
County: Hamilton
License #: 13-35179-02
Agreement: N
Docket:
NRC Notified By: Matthew Trusner
HQ OPS Officer: Tenisha Meadows
Notification Date: 04/09/2025
Notification Time: 09:54 [ET]
Event Date: 04/08/2025
Event Time: 15:18 [EDT]
Last Update Date: 04/09/2025
Notification Time: 09:54 [ET]
Event Date: 04/08/2025
Event Time: 15:18 [EDT]
Last Update Date: 04/09/2025
Emergency Class: Non Emergency
10 CFR Section:
20.2202(b)(1) - Pers Overexposure/TEDE >= 5 Rem
10 CFR Section:
20.2202(b)(1) - Pers Overexposure/TEDE >= 5 Rem
Person (Organization):
Hills, David (R3DO)
NMSS_EVENTS_NOTIFICATION (EMAIL)
Hills, David (R3DO)
NMSS_EVENTS_NOTIFICATION (EMAIL)
POSSIBLE OVEREXPOSURE DUE TO LOSS OF CONTROL OF LICENSED MATERIAL
The following information was provided by the licensee via phone and email:
"At 1518 EDT on April 8, 2025, the radiation safety officer (RSO) was informed about an incident that happened during routine Sr-82 production and waste activities. Four workers were performing waste and remediation activities for a Sr-82 production hot cell. The work was performed under a job-specific radiation work permit and direct supervision of health physics staff. Two of the workers (Worker 1 and Worker 2) entered the waste collection space (basement) located underneath the hot cell to repair a clog in the solid waste duct and replace the liquid acid waste transfer container. Worker 1 and Worker 2 were wearing positive air pressure respirators (PAPRs) which are the appropriate personal protective equipment for work being performed and electronic dosimeters. Worker 2 surveyed the working area upon entry and the shielded waste container using a RadEye [survey meter]. Worker 2 found a partially unshielded area in the waste container reading 930 mR/hr (highest reading recorded during survey).
"Worker 1 and Worker 2 proceeded to disconnect the solid waste duct to remove a potential clog and inspected the waste container. The solid waste container was empty. While inspecting the solid waste duct, a liquid acid waste line disconnected from the bottom of the hot cell. There was no liquid in the line. Worker 1 moved the solid waste cask out of the way of the work area. Worker 1 and Worker 2 then focused on the liquid acid waste container. Worker 1 and Worker 2 moved the shielded acid waste container to the entry of the waste area and removed the lid of the container. Worker 2 removed the plastic bag from the waste container and placed it away from the working area. Worker 1 then replaced the liquid acid waste bucket.
"Worker 1 and Worker 2 returned to the solid waste chute to inspect and unclog the chute. The second liquid waste line broke at this time and fell to the floor. Worker 1 and Worker 2 returned to the entry way and communicated the problem to Worker 3 and Worker 4. It was requested that Worker 3 attempt to lift the waste plate inside the hot cell to reconnect the waste lines and lower the lines back into the waste area. A survey of the hot cell was requested prior to starting this work. Worker 3 opened the hot cell and found the working area to read between 1.5 R/hr to 5 R/hr. Worker 3 unsuccessfully tried to open the connection plate between the hot cell and the solid waste duct. Worker 1 and Worker 2 positioned the shielded waste cask under the hot cell to reconnect it to the hot cell. Worker 1 and Worker 2 noted the dose alarms (100 mrem threshold) on their dosimeters at this time. When they were unsuccessful in lifting the shielded cask into position, they abandoned the work and exited the waste collection space. Upon exiting, their electronic dosimeters were alarming. Worker 1 and Worker 2 noted that their electronic dosimeters were alarming and recorded doses of 4.399 rem for Worker 1 and 2.924 rem for Worker 2.
"Worker 2 escalated the incident to the RSO immediately. The RSO secured the area and instructed Worker 4 to survey the space between the hot cell and the solid waste plate that connects the solid waste duct. Worker 4 found the exposure rates to be 75 mR/hr. As a post-incident follow-up, the RSO instructed Worker 3 to enter the waste collection space to confirm the exposure rates. Worker 3 found exposure rates of 2 R/hr at the entry point, 25 R/hr next to the working location and a waste bucket opposite to the working area that saturated the detector (>1,000 R/hr on contact). Worker 3 electronic dosimeter recorded a dose of 457 mrem. Worker 1 exhibited a maximum of 25,000 disintegrations per minute (dpm) on their left hand. Worker 4 exhibited a maximum of 1,200 counts per minute (120 dpm) on his shirt. Preliminary urinalysis results for Worker 1 did not identify count rates above background levels (no intake).
"The RSO initiated a stop work for production waste activities. As a post-incident follow-up, the director of the radiation safety office and RSO immediately reviewed the dose to date in 2025 and found that Worker 1 total dose was 5.604 rem, exceeding the dose limit set forth in 10 CFR 20.1201. The RSO and director of the radiation safety office initiated a formal investigation."
The following additional information was obtained from the licensee in accordance with Headquarters Operations Officers Report Guidance:
Discussions with the licensee revealed that the report is being submitted pursuant to 10 CFR 20.2202(b)(1)(i) for an individual potentially exceeding a total effective dose equivalent of 5 rem within 24 hours due to a loss of control of licensed material. Additionally, a 30-day report will be submitted pursuant to 10 CFR 20.2203(a)(2)(i) for an adult receiving an annual occupational total effective dose equivalent in excess of 5 rem.
The following information was provided by the licensee via phone and email:
"At 1518 EDT on April 8, 2025, the radiation safety officer (RSO) was informed about an incident that happened during routine Sr-82 production and waste activities. Four workers were performing waste and remediation activities for a Sr-82 production hot cell. The work was performed under a job-specific radiation work permit and direct supervision of health physics staff. Two of the workers (Worker 1 and Worker 2) entered the waste collection space (basement) located underneath the hot cell to repair a clog in the solid waste duct and replace the liquid acid waste transfer container. Worker 1 and Worker 2 were wearing positive air pressure respirators (PAPRs) which are the appropriate personal protective equipment for work being performed and electronic dosimeters. Worker 2 surveyed the working area upon entry and the shielded waste container using a RadEye [survey meter]. Worker 2 found a partially unshielded area in the waste container reading 930 mR/hr (highest reading recorded during survey).
"Worker 1 and Worker 2 proceeded to disconnect the solid waste duct to remove a potential clog and inspected the waste container. The solid waste container was empty. While inspecting the solid waste duct, a liquid acid waste line disconnected from the bottom of the hot cell. There was no liquid in the line. Worker 1 moved the solid waste cask out of the way of the work area. Worker 1 and Worker 2 then focused on the liquid acid waste container. Worker 1 and Worker 2 moved the shielded acid waste container to the entry of the waste area and removed the lid of the container. Worker 2 removed the plastic bag from the waste container and placed it away from the working area. Worker 1 then replaced the liquid acid waste bucket.
"Worker 1 and Worker 2 returned to the solid waste chute to inspect and unclog the chute. The second liquid waste line broke at this time and fell to the floor. Worker 1 and Worker 2 returned to the entry way and communicated the problem to Worker 3 and Worker 4. It was requested that Worker 3 attempt to lift the waste plate inside the hot cell to reconnect the waste lines and lower the lines back into the waste area. A survey of the hot cell was requested prior to starting this work. Worker 3 opened the hot cell and found the working area to read between 1.5 R/hr to 5 R/hr. Worker 3 unsuccessfully tried to open the connection plate between the hot cell and the solid waste duct. Worker 1 and Worker 2 positioned the shielded waste cask under the hot cell to reconnect it to the hot cell. Worker 1 and Worker 2 noted the dose alarms (100 mrem threshold) on their dosimeters at this time. When they were unsuccessful in lifting the shielded cask into position, they abandoned the work and exited the waste collection space. Upon exiting, their electronic dosimeters were alarming. Worker 1 and Worker 2 noted that their electronic dosimeters were alarming and recorded doses of 4.399 rem for Worker 1 and 2.924 rem for Worker 2.
"Worker 2 escalated the incident to the RSO immediately. The RSO secured the area and instructed Worker 4 to survey the space between the hot cell and the solid waste plate that connects the solid waste duct. Worker 4 found the exposure rates to be 75 mR/hr. As a post-incident follow-up, the RSO instructed Worker 3 to enter the waste collection space to confirm the exposure rates. Worker 3 found exposure rates of 2 R/hr at the entry point, 25 R/hr next to the working location and a waste bucket opposite to the working area that saturated the detector (>1,000 R/hr on contact). Worker 3 electronic dosimeter recorded a dose of 457 mrem. Worker 1 exhibited a maximum of 25,000 disintegrations per minute (dpm) on their left hand. Worker 4 exhibited a maximum of 1,200 counts per minute (120 dpm) on his shirt. Preliminary urinalysis results for Worker 1 did not identify count rates above background levels (no intake).
"The RSO initiated a stop work for production waste activities. As a post-incident follow-up, the director of the radiation safety office and RSO immediately reviewed the dose to date in 2025 and found that Worker 1 total dose was 5.604 rem, exceeding the dose limit set forth in 10 CFR 20.1201. The RSO and director of the radiation safety office initiated a formal investigation."
The following additional information was obtained from the licensee in accordance with Headquarters Operations Officers Report Guidance:
Discussions with the licensee revealed that the report is being submitted pursuant to 10 CFR 20.2202(b)(1)(i) for an individual potentially exceeding a total effective dose equivalent of 5 rem within 24 hours due to a loss of control of licensed material. Additionally, a 30-day report will be submitted pursuant to 10 CFR 20.2203(a)(2)(i) for an adult receiving an annual occupational total effective dose equivalent in excess of 5 rem.
Non-Agreement State
Event Number: 57660
Rep Org: Dupont Specialty Products USA LLC
Licensee: Dupont Specialty Products USA LLC
Region: 1
City: Wilmington State: DE
County:
License #: 07-13441-02
Agreement: N
Docket:
NRC Notified By: John Brisbin
HQ OPS Officer: Josue Ramirez
Licensee: Dupont Specialty Products USA LLC
Region: 1
City: Wilmington State: DE
County:
License #: 07-13441-02
Agreement: N
Docket:
NRC Notified By: John Brisbin
HQ OPS Officer: Josue Ramirez
Notification Date: 04/10/2025
Notification Time: 12:41 [ET]
Event Date: 03/27/2025
Event Time: 00:00 [EDT]
Last Update Date: 04/10/2025
Notification Time: 12:41 [ET]
Event Date: 03/27/2025
Event Time: 00:00 [EDT]
Last Update Date: 04/10/2025
Emergency Class: Non Emergency
10 CFR Section:
20.2201(a)(1)(i) - Lost/Stolen LNM>1000x
10 CFR Section:
20.2201(a)(1)(i) - Lost/Stolen LNM>1000x
Person (Organization):
Schussler, Jason (R1DO)
Vossmar, Patricia (R4DO)
NMSS_Events_Notification, (EMAIL)
ILTAB, (EMAIL)
CNSNS (Mexico), - (EMAIL) (EMAIL)
Schussler, Jason (R1DO)
Vossmar, Patricia (R4DO)
NMSS_Events_Notification, (EMAIL)
ILTAB, (EMAIL)
CNSNS (Mexico), - (EMAIL) (EMAIL)
THEFT OR LOSS OF LICENSED MATERIAL
The following is a summary of the information provided by the licensee via phone:
During a shipment from Wilmington, Delaware to Albuquerque, New Mexico, a 0.63 millicurie iron-55 (Fe-55) source was lost or stolen in transit. The last known location was Wilmington, Delaware. The source was shipped on March 27, 2025, and was identified as lost on April 10, 2025. The shipping package was delivered to the intended recipient, but the shipping package was compromised with the source missing. The shipper and the common carrier are investigating.
Model Number: FE5VZ29120005M
Serial Number: NK772
THIS MATERIAL EVENT CONTAINS A 'Less than Cat 3' LEVEL OF RADIOACTIVE MATERIAL
Sources that are "Less than IAEA Category 3 sources," are either sources that are very unlikely to cause permanent injury to individuals or contain a very small amount of radioactive material that would not cause any permanent injury. Some of these sources, such as moisture density gauges or thickness gauges that are Category 4, the amount of unshielded radioactive material, if not safely managed or securely protected, could possibly - although it is unlikely - temporarily injure someone who handled it or were otherwise in contact with it, or who were close to it for a period of many weeks. For additional information go to http://www-pub.iaea.org/MTCD/publications/PDF/Pub1227_web.pdf
The following is a summary of the information provided by the licensee via phone:
During a shipment from Wilmington, Delaware to Albuquerque, New Mexico, a 0.63 millicurie iron-55 (Fe-55) source was lost or stolen in transit. The last known location was Wilmington, Delaware. The source was shipped on March 27, 2025, and was identified as lost on April 10, 2025. The shipping package was delivered to the intended recipient, but the shipping package was compromised with the source missing. The shipper and the common carrier are investigating.
Model Number: FE5VZ29120005M
Serial Number: NK772
THIS MATERIAL EVENT CONTAINS A 'Less than Cat 3' LEVEL OF RADIOACTIVE MATERIAL
Sources that are "Less than IAEA Category 3 sources," are either sources that are very unlikely to cause permanent injury to individuals or contain a very small amount of radioactive material that would not cause any permanent injury. Some of these sources, such as moisture density gauges or thickness gauges that are Category 4, the amount of unshielded radioactive material, if not safely managed or securely protected, could possibly - although it is unlikely - temporarily injure someone who handled it or were otherwise in contact with it, or who were close to it for a period of many weeks. For additional information go to http://www-pub.iaea.org/MTCD/publications/PDF/Pub1227_web.pdf
Agreement State
Event Number: 57662
Rep Org: California Radiation Control Prgm
Licensee: Hoag Memorial Hospital Presbyterian
Region: 4
City: Newport Beach State: CA
County:
License #: 0272-30
Agreement: Y
Docket:
NRC Notified By: Robert Greger
HQ OPS Officer: Ian Howard
Licensee: Hoag Memorial Hospital Presbyterian
Region: 4
City: Newport Beach State: CA
County:
License #: 0272-30
Agreement: Y
Docket:
NRC Notified By: Robert Greger
HQ OPS Officer: Ian Howard
Notification Date: 04/11/2025
Notification Time: 21:25 [ET]
Event Date: 03/26/2025
Event Time: 00:00 [PDT]
Last Update Date: 04/11/2025
Notification Time: 21:25 [ET]
Event Date: 03/26/2025
Event Time: 00:00 [PDT]
Last Update Date: 04/11/2025
Emergency Class: Non Emergency
10 CFR Section:
Agreement State
10 CFR Section:
Agreement State
Person (Organization):
Vossmar, Patricia (R4DO)
NMSS_EVENTS_NOTIFICATION (EMAIL)
Vossmar, Patricia (R4DO)
NMSS_EVENTS_NOTIFICATION (EMAIL)
AGREEMENT STATE REPORT - MEDICAL EVENT
"The licensee initially reported an underdose event that involved a CyberKnife (linear accelerator), and the event was referred to our X-ray inspection unit. On 4/11/25, our X-ray unit informed us that the underdose event involved an Elekta Gamma Knife Perfexion (Co-60) that experienced an electrical sensor failure that caused the patient's treatment to be interrupted.
"The original planned treatment using stereotactic radiosurgery to the right trigeminal nerve using a single 4 mm collimator open shot to deliver a maximum of 80 Gy (76 Gy at the 95 percent isodose line). The treatment time was to take 49.24 minutes. However, after 12.47 minutes of treatment, a system error on the GK unit triggered a stop in treatment. All radiation sources (Co-60) were retracted to home positions and the patient was automatically removed from the treatment bore by the robotic couch with the shielding doors automatically closing. The patient only received 25 percent of the dose on 3/26/25, or about 20 Gy.
"On 3/27/25, the machine was successfully repaired by an Elekta engineer and the patient came back to the facility to complete treatment. The authorized user physicians modified their written directive and treatment plan to give an additional maximum dose of 70 Gy (66.5 Gy at the 95 percent isodose line) to the same treatment area. The patient successfully completed the treatment."
California 5010 Number: 032625
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.
"The licensee initially reported an underdose event that involved a CyberKnife (linear accelerator), and the event was referred to our X-ray inspection unit. On 4/11/25, our X-ray unit informed us that the underdose event involved an Elekta Gamma Knife Perfexion (Co-60) that experienced an electrical sensor failure that caused the patient's treatment to be interrupted.
"The original planned treatment using stereotactic radiosurgery to the right trigeminal nerve using a single 4 mm collimator open shot to deliver a maximum of 80 Gy (76 Gy at the 95 percent isodose line). The treatment time was to take 49.24 minutes. However, after 12.47 minutes of treatment, a system error on the GK unit triggered a stop in treatment. All radiation sources (Co-60) were retracted to home positions and the patient was automatically removed from the treatment bore by the robotic couch with the shielding doors automatically closing. The patient only received 25 percent of the dose on 3/26/25, or about 20 Gy.
"On 3/27/25, the machine was successfully repaired by an Elekta engineer and the patient came back to the facility to complete treatment. The authorized user physicians modified their written directive and treatment plan to give an additional maximum dose of 70 Gy (66.5 Gy at the 95 percent isodose line) to the same treatment area. The patient successfully completed the treatment."
California 5010 Number: 032625
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.
Fuel Cycle Facility
Event Number: 57664
Facility: Westinghouse Electric Corporation
Region: 2 State: SC
Unit: [] [] []
RX Type: Uranium Fuel Fabrication
NRC Notified By: Steve Subosits
HQ OPS Officer: Ian Howard
Region: 2 State: SC
Unit: [] [] []
RX Type: Uranium Fuel Fabrication
NRC Notified By: Steve Subosits
HQ OPS Officer: Ian Howard
Notification Date: 04/13/2025
Notification Time: 17:07 [ET]
Event Date: 04/13/2025
Event Time: 02:15 [EDT]
Last Update Date: 04/13/2025
Notification Time: 17:07 [ET]
Event Date: 04/13/2025
Event Time: 02:15 [EDT]
Last Update Date: 04/13/2025
Emergency Class: Non Emergency
10 CFR Section:
70.50(b)(3) - Med Treat Involving Contam
10 CFR Section:
70.50(b)(3) - Med Treat Involving Contam
Person (Organization):
Pearson, Laura (R2DO)
Helton, Shana (NMSS)
Crouch, Howard (IR)
NMSS_Events_Notification, (EMAIL)
Pearson, Laura (R2DO)
Helton, Shana (NMSS)
Crouch, Howard (IR)
NMSS_Events_Notification, (EMAIL)
MEDICAL TRANSPORT WITH CONTAMINATION
The following information was provided by the licensee via phone and email:
"At approximately 0215 EDT, on April 13, 2025, a uranium recovery and recycle services (URRS) operator was performing a pressure check of a dissolver system filter housing following change out of the filter cartridges. Uranyl nitrate solution discharged from the housing lid/housing body interface onto the operator's coveralls in the upper left arm area. In accordance with the operating procedure, the operator was wearing a full-face shield, safety glasses, chemical gloves, and a chemical apron that covers the torso area. The chemical apron does not cover the arm area.
"The operator reported the exposure to a URRS chief operator and the skin area on the upper left arm was rinsed for approximately fifteen minutes. The incident commander, a medical first responder from the Columbia Fuel Fabrication Facility (CFFF) emergency brigade and a health physics (HP) technician were contacted to respond to the URRS area. After decontamination efforts on the affected area of the arm, HP direct [on contact] survey results were 500 disintegrations per minute (dpm) per 100 cm squared of alpha [radiation] for the left bicep area.
"The filter housing lid was secured properly and passed the pressure check required by the operating procedure. This event did not impact safety equipment. A causal analysis and corrective actions will be documented in the Corrective Action Program (CAP).
"All smear survey results of the exposed skin area were below clean area limits (less than 200 dpm per 100 cm squared). As a precaution to ensure comprehensive evaluation and treatment for uranyl nitrate/nitric acid exposure to the skin, the operator was transported by ambulance to an offsite medical facility. The affected portion of the employee's arm was bandaged and wrapped in gauze and tape, and the employee was accompanied by a CFFF HP technician for evaluation. Contamination surveys were performed for the ambulance and the gurney used to transport the employee, and all results were below clean area limits, indicating no spread of contamination during care for the employee. All potentially contaminated materials associated with the transport were collected and returned to the CFFF for disposal. The employee was provided with an over-the-counter topical ointment and released from the offsite medical facility at 0735 on April 13, 2025.
"The CFFF is a licensed Part 70 facility subject to 10 CFR 70 Subpart H, and the event did not challenge the performance requirements of 10 CFR 70.61 as analyzed in the Integrated Safety Analysis."
The following information was provided by the licensee via phone and email:
"At approximately 0215 EDT, on April 13, 2025, a uranium recovery and recycle services (URRS) operator was performing a pressure check of a dissolver system filter housing following change out of the filter cartridges. Uranyl nitrate solution discharged from the housing lid/housing body interface onto the operator's coveralls in the upper left arm area. In accordance with the operating procedure, the operator was wearing a full-face shield, safety glasses, chemical gloves, and a chemical apron that covers the torso area. The chemical apron does not cover the arm area.
"The operator reported the exposure to a URRS chief operator and the skin area on the upper left arm was rinsed for approximately fifteen minutes. The incident commander, a medical first responder from the Columbia Fuel Fabrication Facility (CFFF) emergency brigade and a health physics (HP) technician were contacted to respond to the URRS area. After decontamination efforts on the affected area of the arm, HP direct [on contact] survey results were 500 disintegrations per minute (dpm) per 100 cm squared of alpha [radiation] for the left bicep area.
"The filter housing lid was secured properly and passed the pressure check required by the operating procedure. This event did not impact safety equipment. A causal analysis and corrective actions will be documented in the Corrective Action Program (CAP).
"All smear survey results of the exposed skin area were below clean area limits (less than 200 dpm per 100 cm squared). As a precaution to ensure comprehensive evaluation and treatment for uranyl nitrate/nitric acid exposure to the skin, the operator was transported by ambulance to an offsite medical facility. The affected portion of the employee's arm was bandaged and wrapped in gauze and tape, and the employee was accompanied by a CFFF HP technician for evaluation. Contamination surveys were performed for the ambulance and the gurney used to transport the employee, and all results were below clean area limits, indicating no spread of contamination during care for the employee. All potentially contaminated materials associated with the transport were collected and returned to the CFFF for disposal. The employee was provided with an over-the-counter topical ointment and released from the offsite medical facility at 0735 on April 13, 2025.
"The CFFF is a licensed Part 70 facility subject to 10 CFR 70 Subpart H, and the event did not challenge the performance requirements of 10 CFR 70.61 as analyzed in the Integrated Safety Analysis."
Power Reactor
Event Number: 57673
Facility: McGuire
Region: 2 State: NC
Unit: [1] [] []
RX Type: [1] W-4-LP,[2] W-4-LP
NRC Notified By: Just Selepec
HQ OPS Officer: Ian Howard
Region: 2 State: NC
Unit: [1] [] []
RX Type: [1] W-4-LP,[2] W-4-LP
NRC Notified By: Just Selepec
HQ OPS Officer: Ian Howard
Notification Date: 04/20/2025
Notification Time: 08:01 [ET]
Event Date: 04/20/2025
Event Time: 00:28 [EDT]
Last Update Date: 04/20/2025
Notification Time: 08:01 [ET]
Event Date: 04/20/2025
Event Time: 00:28 [EDT]
Last Update Date: 04/20/2025
Emergency Class: Non Emergency
10 CFR Section:
50.72(b)(3)(v)(D) - Accident Mitigation
10 CFR Section:
50.72(b)(3)(v)(D) - Accident Mitigation
Person (Organization):
Pearson, Laura (R2DO)
Pearson, Laura (R2DO)
| Unit | SCRAM Code | RX Crit | Initial PWR | Initial RX Mode | Current PWR | Current RX Mode |
|---|---|---|---|---|---|---|
| 1 | N | N | 0 | 0 |
EMERGENCY CORE COOLING SYSTEM (ECCS) ACCUMULATORS INOPERABLE
The following information was provided by the licensee via phone and email:
"At 0028 EDT on 4/20/2025, it was discovered that all trains of the ECCS accumulators were simultaneously inoperable. Therefore, this condition is being reported as an eight-hour, non-emergency notification per 10 CFR 50.72(b)(3)(v). The safety function was restored at 0028 on 04/20/2025 and all required trains have been declared operable. There was no impact to the other unit.
"There was no impact on the health and safety of the public or plant personnel. The NRC Resident Inspector has been notified."
The following additional information was obtained from the licensee in accordance with Headquarters Operations Officers Report Guidance:
The sample lines for each accumulator cold leg were open for inspection, which crossties the cold leg accumulator gas spaces. Upon discovery of this condition, the sample lines were subsequently closed, and the accumulators were declared operable.
The following information was provided by the licensee via phone and email:
"At 0028 EDT on 4/20/2025, it was discovered that all trains of the ECCS accumulators were simultaneously inoperable. Therefore, this condition is being reported as an eight-hour, non-emergency notification per 10 CFR 50.72(b)(3)(v). The safety function was restored at 0028 on 04/20/2025 and all required trains have been declared operable. There was no impact to the other unit.
"There was no impact on the health and safety of the public or plant personnel. The NRC Resident Inspector has been notified."
The following additional information was obtained from the licensee in accordance with Headquarters Operations Officers Report Guidance:
The sample lines for each accumulator cold leg were open for inspection, which crossties the cold leg accumulator gas spaces. Upon discovery of this condition, the sample lines were subsequently closed, and the accumulators were declared operable.