SELENIA MAMMOGRAPHY SYSTEM SEL-00002

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-03 for SELENIA MAMMOGRAPHY SYSTEM SEL-00002 manufactured by Hologic, Inc.

Event Text Entries

[182319498] As of today the investigation is still in process and a follow up will be filed as needed.
Patient Sequence No: 1, Text Type: N, H10


[182319499] It was reported that the c-arm is not parallel with the gantry and metal shavings are seen on the rotation collar. No injury reported. A field engineer was dispatched to the site.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1220984-2020-00035
MDR Report Key9781750
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-03
Date of Report2020-02-03
Date of Event2020-02-03
Date Mfgr Received2020-02-03
Device Manufacturer Date2007-03-01
Date Added to Maude2020-03-03
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKRISTIN FORNIERI
Manufacturer Street36 & 37 APPLE RIDGE ROAD
Manufacturer CityDANBURY, CT
Manufacturer CountryUS
Manufacturer Phone7318491
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSELENIA MAMMOGRAPHY SYSTEM
Generic NameFULL FIELD DIGITAL MAMMOGRAPHY SYSTEM
Product CodeMUE
Date Received2020-03-03
Model NumberSEL-00002
Catalog NumberSEL-00002
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerHOLOGIC, INC
Manufacturer Address36 & 37 APPLE RIDGE ROAD DANBURY, CT US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-03

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