DISCOVERY DISCOVERY-W N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2018-01-10 for DISCOVERY DISCOVERY-W N/A manufactured by Hologic, Inc.

Event Text Entries

[96945234] It was reported that the system received an error at the end of scan which prevented the scan from being viewable and caused the patient to be re-exposed. It was determined that an odbc database repair was needed. Once the odbc database repair was completed the system is working as intended.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1220984-2018-00056
MDR Report Key7180408
Report SourceUSER FACILITY
Date Received2018-01-10
Date of Report2018-01-09
Date of Event2017-12-06
Date Mfgr Received2018-01-09
Device Manufacturer Date2015-01-21
Date Added to Maude2018-01-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationSERVICE PERSONNEL
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 NameDISCOVERY
Generic NameDENSITOMETER, BONE
Product CodeKGI
Date Received2018-01-10
Model NumberDISCOVERY-W
Catalog NumberN/A
Lot NumberN/A
OperatorRADIOLOGIC TECHNOLOGIST
Device AvailabilityY
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 2018-01-10

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