A-SPOT 651

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 2015-12-17 for A-SPOT 651 manufactured by Beekley Corporation.

Event Text Entries

[33741725] A palpable mass marker may have caused artifact on a mammogram. As a result, the mammogram was repeated.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9021987-2015-00006
MDR Report Key5306038
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2015-12-17
Date of Report2015-12-17
Date of Event2015-11-17
Date Mfgr Received2015-11-24
Device Manufacturer Date2014-09-24
Date Added to Maude2015-12-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRADIOLOGIC TECHNOLOGIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKATE CHASE
Manufacturer Street1 PRESTIGE LANE
Manufacturer CityBRISTOL CT 06010
Manufacturer CountryUS
Manufacturer Postal06010
Manufacturer Phone8605834700
Manufacturer G1BEEKLEY CORPORATION
Manufacturer Street1 PRESTIGE LANE
Manufacturer CityBRISTOL CT 06010
Manufacturer CountryUS
Manufacturer Postal Code06010
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameA-SPOT
Generic NamePALPABLE MASS MARKER
Product CodeJAC
Date Received2015-12-17
Returned To Mfg2015-12-15
Model Number651
Catalog Number651
Lot Number651.09251402
OperatorRADIOLOGIC TECHNOLOGIST
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBEEKLEY CORPORATION
Manufacturer Address1 PRESTIGE LANE BRISTOL CT 06010 US 06010


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-12-17

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