MULTICARE PLATINUM 8-004-0017

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 2019-01-04 for MULTICARE PLATINUM 8-004-0017 manufactured by Hologic, Inc.

Event Text Entries

[132226113] It was reported that the table will lower on its own after they raise it up to the top of travel. No injury reported. A field engineer was dispatched to the site and determined that the table down switch on the control panel membrane switch bank was shorted out. The control panel membrane switch was replaced. Once this was completed the system was working as intended.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1220984-2019-00002
MDR Report Key8218287
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-01-04
Date of Report2018-12-07
Date of Event2018-12-07
Date Mfgr Received2018-12-07
Device Manufacturer Date2008-12-01
Date Added to Maude2019-01-04
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 NameMULTICARE PLATINUM
Generic NameSTEREOTACTIC BREAST BIOPSY SYSTEM
Product CodeIZH
Date Received2019-01-04
Model Number8-004-0017
Catalog Number8-004-0017
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 2019-01-04

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