SELENIA MAMMOGRAPHY SYSTEM SEL-00014

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-20 for SELENIA MAMMOGRAPHY SYSTEM SEL-00014 manufactured by Hologic, Inc.

Event Text Entries

[184442468] It was reported that the technologist presses the c-arm angle button and the c-arm continues to move. No injury reported. A field engineer was dispatched to the site and determined the rotation button housing needed to be adjusted. Once this was completed the system was working as intended.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1220984-2020-00043
MDR Report Key9861187
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-03-20
Date of Report2020-03-02
Date of Event2020-03-02
Date Mfgr Received2020-03-02
Device Manufacturer Date2008-11-01
Date Added to Maude2020-03-20
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
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 Received2020-03-20
Model NumberSEL-00014
Catalog NumberSEL-00014
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 US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-20

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