AFFIRM BREAST BIOPSY GUIDANCE SYSTEM STLC-00004

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-01-21 for AFFIRM BREAST BIOPSY GUIDANCE SYSTEM STLC-00004 manufactured by Hologic, Inc.

Event Text Entries

[178640296] It was reported that the affirm crashed during biopsy, after re-targeting more than 1 cm. No injury reported. A field engineer was dispatched to the site and determined the bcm, bgm pcb, and bgm cable needed to be replaced. Once this was completed the system was working as intended.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1220984-2020-00007
MDR Report Key9612751
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2020-01-21
Date Mfgr Received2019-12-31
Device Manufacturer Date2014-12-01
Date Added to Maude2020-01-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKRISTIN FORNIERI
Manufacturer Street36 & 37 APPLE RIDGE ROAD
Manufacturer CityDANBURY CT 06810
Manufacturer CountryUS
Manufacturer Postal06810
Manufacturer Phone2037318491
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAFFIRM BREAST BIOPSY GUIDANCE SYSTEM
Generic NameBIOPSY GUIDANCE SYSTEM
Product CodeIZH
Date Received2020-01-21
Model NumberSTLC-00004
Catalog NumberSTLC-00004
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerHOLOGIC, INC
Manufacturer Address36 & 37 APPLE RIDGE ROAD DANBURY CT 06810 US 06810


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-21

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