CODMAN EXT DRAINAGE SYSTEM III WITHOUT VENT CATH 821731

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 2019-01-29 for CODMAN EXT DRAINAGE SYSTEM III WITHOUT VENT CATH 821731 manufactured by Natus Neuro Incorporated.

Event Text Entries

[134414064] Reference (b)(4). Investigation incomplete, waiting for return of device.
Patient Sequence No: 1, Text Type: N, H10


[134414065] Connection to the patient became cracked, allowing air into the system and intercranial ventricles.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010611950-2019-00002
MDR Report Key8287371
Report SourceUSER FACILITY
Date Received2019-01-29
Date of Report2019-01-15
Date of Event2018-12-11
Date Mfgr Received2019-01-15
Date Added to Maude2019-01-29
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. JANESSA BOONE
Manufacturer Street3150 PLEASANT VIEW ROAD
Manufacturer CityMIDDLETON WI 53562
Manufacturer CountryUS
Manufacturer Postal53562
Manufacturer Phone6088298603
Manufacturer G1NATUS NEUROLOGY INCORPORATED
Manufacturer Street5955 PACIFIC CENTER BOULEVARD
Manufacturer CitySAN DIEGO CA 92121
Manufacturer CountryUS
Manufacturer Postal Code92121
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCODMAN EXT DRAINAGE SYSTEM III WITHOUT VENT CATH
Generic NameSHUNT, CENTRAL NERVOUS SYSTEM & COMPS
Product CodePSP
Date Received2019-01-29
Model Number821731
Catalog Number821731
Lot Number207532
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNATUS NEURO INCORPORATED
Manufacturer Address3150 PLEASANT VIEW ROAD MIDDLETON WI 53562 US 53562


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-01-29

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