MAUDE Adverse Event Report: HOLOGIC, INC. SELENIA DIMENSIONS AVIA; MAMMOGRAPHY SYSTEM

Model Number	SDA-SYS-3000-2D-CN
Medical Device Problem Code	Unintended System Motion (1430)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/16/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that a selenia dimension procedure on june 16th, and the c-arm rotation switch did not work during the process.A field engineer examined the equipment and determined that the rotation switch under the c-arm was defective, the c-arm rotates even when the switch is released.The switch was replaced.The system passed all tests and meets the manufacturer´s specifications.No patient or staff injury was reported.No other information is available.

• Brand Name: SELENIA DIMENSIONS AVIA
• Common Device Name: MAMMOGRAPHY SYSTEM
• Manufacturer (Section D): HOLOGIC, INC.; 36 & 37 apple ridge road; danbury CT 06810
• Manufacturer (Section G): HOLOGIC, INC.; 36 & 37 apple ridge road; danbury CT 06810
• Manufacturer Contact: ariel lafuente ; 562 parkway; coyol free zone building b24; san jose 20102 ; CR 20102
• MDR Report Key: 17266432
• Report Number: 1220984-2023-00055
• Device Sequence Number: 20848489
• Product Code: OTE
• UDI-Device Identifier: 15420045505636
• UDI-Public: 15420045505636
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: P010025
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 07/06/2023

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: SDA-SYS-3000-2D-CN
• Device Catalogue Number: ASY-04160
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/16/2023
• Initial Report FDA Received Date: 07/06/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/23/2022
• Is the Device Labeled for Single Use? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown