MAUDE Adverse Event Report: SIEMENS HEALTHINEERS AG MAMMOMAT REVELATION; FULL FIELD DIGITAL, SYSTEM, X-RAY, MAMMOGRAPHIC

Model Number	11343300
Medical Device Problem Code	Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/11/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Manufacturer's preliminary results: this equipment was potentially not approved for installation in the bus/truck.During the investigation of another complaint, siemens reference number (b)(4), mdr #3004977335-2025-00066, an analysis in regard to number of occurrences in the installed base and the associated risk was performed.Regarding the associated risk, the recently obtained knowledge acknowledges that it cannot be completely excluded that the monitor might fall off during use and might cause in a worst-case, a serious injury.Initial actions (corrective and/or preventive): currently the issue is under investigation and therefore no immediate actions could be defined at this point in time.However, it is recommended in the system operator manual to check the correct fastening of the monitor and the monitor holder before each use after transportation, and to fasten the screws if necessary.The root cause has not been identified.A supplemental report will be submitted to the fda if additional information becomes available upon completion of the investigation.
Event or Problem Description
Siemens healthineers became aware of an issue with the mammomat revelation system in truck/ bus installation.It was stated that during transit, the front panel of the system monitor installed in the mobile truck, fell down.There were no injuries resulting from the event.In a worst-case scenario, if the event issue were to recur, serious injury could result from a person being hit by falling parts.
Additional Manufacturer Narrative
H3, h6: siemens healthineers completed the detailed investigation of the reported issue.It was stated that during transportation the monitor had fallen and broke into two pieces.During complaint investigation it was determined that the operator table (material number 10549892) was installed in this mobile system.The operator table is not released for mobile systems.The operator table and all attached components are not designed to withstand the loads encountered in a truck due to vibrations.For mobile systems a separate radiation protection shield is available.This is also described in the ¿site planning guide¿.In general, the ordering process for stationary systems is not the same as the ordering process for mobile systems to ensure that not released components (e.G.The operator table) cannot be ordered for mobile vehicles.An individual change can only be manually approved.Therefore, an appropriate retraining of the order team was already initiated.The documents "system/installation and startup instruction" and the "system / site planning guide" were checked and found to be sufficient.The affected customers will be informed about the potential risk when transporting the operator table in bus-installations.The complaint is closed with this statement.

• Brand Name: MAMMOMAT REVELATION
• Common Device Name: FULL FIELD DIGITAL, SYSTEM, X-RAY, MAMMOGRAPHIC
• Manufacturer (Section D): SIEMENS HEALTHINEERS AG; siemensstrasse 1; -or- rittigfeld 1; forchheim 91301 ; GM 91301
• Manufacturer (Section G): SIEMENS HEALTHINEERS AG; siemensstrasse 1; -or- rittigfeld 1; forchheim 91301 ; GM 91301
• Manufacturer Contact: rebecca tudor ; 40 liberty blvd.; malvern, PA 91301 ; 4843234198
• MDR Report Key: 22095002
• Report Number: 3004977335-2025-00067
• Device Sequence Number: 7866676
• Product Code: MUE
• UDI-Device Identifier: 04056869124575
• UDI-Public: (01)04056869124575
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K193166
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 09/02/2025

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
• Operator of Device: Health Professional
• Device Model Number: 11343300
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/16/2025
• Supplement Date Received by Manufacturer: 08/29/2025
• Initial Report FDA Received Date: 05/28/2025
• Supplement Report FDA Received Date: 09/02/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 08/29/2025
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: A
• Patient Sequence Number: 1
• Patient Sex: Unknown