TUR IRRIGATION SET 2C4041

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-08-12 for TUR IRRIGATION SET 2C4041 manufactured by Baxter Healthcare - Cartago.

MAUDE Entry Details

Report Number1416980-2019-04373
MDR Report Key8883671
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-08-12
Date of Report2019-09-10
Date of Event2019-07-12
Date Mfgr Received2019-09-03
Device Manufacturer Date2018-07-26
Date Added to Maude2019-08-12
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 - CARTAGO
Manufacturer StreetSEE H10
Manufacturer CityCARTAGO 30106
Manufacturer CountryCS
Manufacturer Postal Code30106
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTUR IRRIGATION SET
Generic NameSYSTEM, IRRIGATION, UROLOGICAL
Product CodeLJH
Date Received2019-08-12
Returned To Mfg2019-07-29
Model NumberNA
Catalog Number2C4041
Lot NumberR18G25028
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE - CARTAGO
Manufacturer AddressCARTAGO


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-12

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