SELENIA DIMENSIONS MAMMOGRAPHY SYSTEM SDM-00001-2D

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 2020-01-09 for SELENIA DIMENSIONS MAMMOGRAPHY SYSTEM SDM-00001-2D manufactured by Hologic, Inc.

Event Text Entries

[178761358] It was reported that they are getting an error message that states left side of c-arm disabled. Additional information obtained confirmed that there was continued motion after the switch was released. No injury reported. A field engineer was dispatched to the site and determined the left and right switch panels 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 Number1220984-2020-00003
MDR Report Key9568563
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-01-09
Date of Report2019-12-20
Date of Event2019-12-20
Date Mfgr Received2019-12-20
Device Manufacturer Date2013-06-01
Date Added to Maude2020-01-09
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 NameSELENIA DIMENSIONS MAMMOGRAPHY SYSTEM
Generic NameFULL FIELD DIGITAL MAMMOGRAPHY SYSTEM
Product CodeMUE
Date Received2020-01-09
Model NumberSDM-00001-2D
Catalog NumberSDM-00001-2D
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 2020-01-09

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