MAUDE Adverse Event Report: SIEMENS HEALTHINEERS ACUSON P500; ULTRASOUND DEVICE

Model Number	10785577
Medical Device Problem Code	Power Problem (3010)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/26/2023
Type of Reportable Event	Malfunction
Event or Problem Description
This report is being submitted following a retrospective review performed by siemens ultrasound.In this case: * customer reports system turned off during the middle of an exam.* afib ablation with ice catheter.* no injuries, customer able to complete exam with another ultrasound.
Additional Manufacturer Narrative
This report is being submitted following a retrospective review performed by siemens ultrasound.Investigation was completed and it was found that: the replaced c-part has not been provided.But we can assume the root cause based on the previous investigation results, a damaged component can be inspected in psu.The improvement of psu is implemented into pn 10789435 revision 08 with starting sn (b)(4).The reported psu sn was 10789435 (rev.07).Reference: (b)(4).

• Brand Name: ACUSON P500
• Common Device Name: ULTRASOUND DEVICE
• Manufacturer (Section D): SIEMENS HEALTHINEERS; 22010 south east 51st street; issaquah WA 98029
• Manufacturer (Section G): SIEMENS HEALTHINEERS; 22010 south east 51st street; issaquah WA 98029
• Manufacturer Contact: pragya jai kumar ; 22010 south east 51st street; issaquah, WA 98029
• MDR Report Key: 21291904
• Report Number: 3023245-2025-00014
• Device Sequence Number: 12706576
• Product Code: IYN
• UDI-Device Identifier: 04056869002743
• UDI-Public: (01)04056869002743
• Combination Product (Y/N): N
• Initial Reporter State: UT
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 02/01/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Model Number: 10785577
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 02/03/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown