MAUDE Adverse Event Report: HOLOGIC, INC EVIVA_0910-20; INSTRUMENT, BIOPSY

Model Number	EVIVA_0910-20
Medical Device Problem Code	Material Twisted/Bent (2981)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/09/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
A device history record (dhr) review was conducted for the reported lot number.The device was released meeting all qa specifications.
Event or Problem Description
During an eviva breast biopsy procedure on (b)(6), 2026, the user reports that the device was "not smooth" during use in the "lavage mode." additionally, it is reported that upon completion of the biopsy procedure, it was observed that the needle was bent.No patient harm was reported, and no further information is currently available.

• Brand Name: EVIVA_0910-20
• Common Device Name: INSTRUMENT, BIOPSY
• Manufacturer (Section D): HOLOGIC, INC; 250 campus drive; marlborough MA 01752
• Manufacturer (Section G): HOLOGIC, INC; 250 campus drive; marlborough MA 01752
• Manufacturer Contact: dara smithers ; 600 technology drive; newark, DE 19702
• MDR Report Key: 24742370
• Report Number: 1222780-2026-00150
• Device Sequence Number: 9376603
• Product Code: KNW
• UDI-Device Identifier: 15420045504950
• UDI-Public: (01)15420045504950(17)270702(10)E25G02RF
• Combination Product (Y/N): N
• Initial Reporter Country: HK
• PMA/510(K) Number: K180233
• 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,Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 03/31/2026

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: EVIVA_0910-20
• Device Catalogue Number: EVIVA_0910-20
• Device Lot Number: E25G02RF
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/09/2026
• Initial Report FDA Received Date: 03/31/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 07/02/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown