LEADCARE ULTRA CONSUMABLE 70-8090

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-11-22 for LEADCARE ULTRA CONSUMABLE 70-8090 manufactured by Magellan Diagnostics, Inc..

MAUDE Entry Details

Report Number1218996-2019-00047
MDR Report Key9365035
Report SourceHEALTH PROFESSIONAL
Date Received2019-11-22
Date of Report2019-11-22
Date of Event2014-10-02
Date Mfgr Received2014-10-02
Device Manufacturer Date2014-04-25
Date Added to Maude2019-11-22
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 ContactMS. IVY MARGARET THIONG'O
Manufacturer Street101 BILLERICA AVE BUILDING 4
Manufacturer CityN. BILLERICA MA 01862
Manufacturer CountryUS
Manufacturer Postal01862
Manufacturer Phone9783135480
Manufacturer G1MAGELLAN DIAGNOSTICS, INC.
Manufacturer Street101 BILLERICA AVE BUILDING 4
Manufacturer CityN. BILLERICA MA 01862
Manufacturer CountryUS
Manufacturer Postal Code01862
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLEADCARE ULTRA CONSUMABLE
Generic NameLEADCARE ULTRA TEST KIT
Product CodeDOF
Date Received2019-11-22
Model Number70-8090
Catalog Number70-8090
Lot Number1404AU
Device Expiration Date2015-10-25
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMAGELLAN DIAGNOSTICS, INC.
Manufacturer Address101 BILLERICA AVE. BUILDING 4 N. BILLERICA MA 01862 US 01862


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.