SHUNT TUNNELER 990010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2012-08-14 for SHUNT TUNNELER 990010 manufactured by Integra Neurosciences Implants Sa.

Event Text Entries

[2793366] A shunt tunneler was being used during a ventricular peritoneal (vp) shunt and the surgeon described the tunneler as being "weak and bends," and is not suitable for tunneling. The age and the gender of the pt is unk. The pt was anesthetized and the procedure was delayed for 15 minutes as a result of this issue. The pt was not injured.
Patient Sequence No: 1, Text Type: D, B5


[10123631] The device involved in the reported incident is not expected to be received for eval. An investigation has been initiated based upon the reported info.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9612007-2012-00026
MDR Report Key2701874
Report Source01,05
Date Received2012-08-14
Date of Report2012-08-14
Date of Event2012-07-17
Date Mfgr Received2012-07-24
Date Added to Maude2012-12-03
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 FDA0
Event Location0
Manufacturer ContactLINDA SERENTINO
Manufacturer Street315 ENTERPRISE DRIVE
Manufacturer Phone6099365560
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameSHUNT TUNNELER
Generic NameVALVE ACCESSORIES
Product CodeGYK
Date Received2012-08-14
Catalog Number990010
Lot Number170524
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA NEUROSCIENCES IMPLANTS SA
Manufacturer AddressSOPHIA ANTIPOLIS F-06921 FR F-06921


Patients

Patient NumberTreatmentOutcomeDate
10 2012-08-14

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