CART M

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 2020-03-26 for CART M manufactured by Lenstec Barbados Inc..

MAUDE Entry Details

Report Number9613160-2020-00009
MDR Report Key9885915
Report SourceUSER FACILITY
Date Received2020-03-26
Date of Report2020-03-26
Date of Event2020-02-05
Date Mfgr Received2020-02-27
Device Manufacturer Date2019-11-15
Date Added to Maude2020-03-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JIMMY CHACKO
Manufacturer Street1765 COMMERCE AVE. N.
Manufacturer CityST. PETERSBURG, FL
Manufacturer CountryUS
Manufacturer Phone5712272
Manufacturer G1LENSTEC BARBADOS INC.
Manufacturer StreetAIRPORT COMMERCIAL CENTRE PILGRIM ROAD
Manufacturer CityCHRIST CHURCH,
Manufacturer CountryBB
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCART M
Generic NameCARTRIDGE
Product CodeMSS
Date Received2020-03-26
Lot Number194407
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerLENSTEC BARBADOS INC.
Manufacturer AddressAIRPORT COMMERCIAL CENTRE PILGRIM ROAD CHRIST CHURCH, BB


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-26

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