CARTRIDGE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-11-26 for CARTRIDGE manufactured by Baxter Healthcare - Tijuana Baja.

MAUDE Entry Details

Report Number8030638-2019-00018
MDR Report Key9375784
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-11-26
Date of Report2019-11-26
Date Facility Aware2019-11-03
Report Date2019-11-25
Date Reported to FDA2019-11-25
Date Reported to Mfgr2019-11-25
Date Mfgr Received2019-11-03
Date Added to Maude2019-11-26
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 Street25212 W. ILLINOIS ROUTE 120
Manufacturer CityROUND LAKE IL 60073
Manufacturer CountryUS
Manufacturer Postal60073
Manufacturer Phone2242702068
Manufacturer G1BAXTER HEALTHCARE - TIJUANA BAJA
Manufacturer StreetBLVD PACIFICO 10014 PARQUE INDUSTRIAL PACIFICO
Manufacturer CityTIJUANA BAJA CALIFORNIA CP 22643
Manufacturer CountryMX
Manufacturer Postal CodeCP 22643
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCARTRIDGE
Generic NameSET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE
Product CodeFJK
Date Received2019-11-26
Model NumberNA
Catalog NumberASKU
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE - TIJUANA BAJA
Manufacturer AddressDEERFIELD IL


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-26

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