PROGAV 2.0 SYS W/SA10 A.CONTROL RESERV. FX432T

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 2020-03-17 for PROGAV 2.0 SYS W/SA10 A.CONTROL RESERV. FX432T manufactured by Christoph Miethke Gmbh & Co. Kg.

Event Text Entries

[186617396] Possible lot number 20039562 (to be confirmed). Additional information / investigation results will be provided in a supplemental report, if applicable.
Patient Sequence No: 1, Text Type: N, H10


[186617397] It was reported that there was an issue with the shunt system. The patient was initially implanted with a progav valve with control reservoir. Sometime later, there was difficulty in re-programming noted. The clinical application specialist nor the surgeon could adjust the setting. There was a revision surgery to replace the defective valve. Additional information has been requested (including clarification on event date and awareness dates).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004721439-2020-00071
MDR Report Key9842191
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-17
Date of Report2020-03-17
Date of Event2020-02-04
Date Mfgr Received2020-02-04
Date Added to Maude2020-03-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JOERG KNEBEL
Manufacturer Street2 ULANENWEG
Manufacturer CityPOTSDAM D, 14469
Manufacturer CountryGM
Manufacturer Postal14469
Manufacturer G1CHRISTOPH MIETHKE GMBH & CO. KG
Manufacturer Street2 ULANENWEG
Manufacturer CityPOTSDAM, 14469
Manufacturer CountryGM
Manufacturer Postal Code14469
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePROGAV 2.0 SYS W/SA10 A.CONTROL RESERV.
Generic NameHYDROCEPHALUS MANAGEMENT
Product CodeJXG
Date Received2020-03-17
Model NumberFX432T
Catalog NumberFX432T
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCHRISTOPH MIETHKE GMBH & CO. KG
Manufacturer Address2 ULANENWEG POTSDAM, 14469 GM 14469


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-17

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