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 2013-12-20 for SHUNT TUNNELER 990010 manufactured by Integra Neurosciences Implants S.a..

Event Text Entries

[4342807] It was reported that the tunneler was too soft and too complicated to guide. The product was in contact with the patient. There was no patient injury or death alleged. This event led to an increase in surgery time (exact time not provided). The product was thrown out. Add'l info has been requested.
Patient Sequence No: 1, Text Type: D, B5


[11640135] The device involved in the reported incident is not expected to be received for evaluation. The device was discarded by the customer. An investigation has been initiated based upon the reported info.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9612007-2013-00028
MDR Report Key3663245
Report Source01,05
Date Received2013-12-20
Date of Report2013-12-05
Date Mfgr Received2013-12-05
Date Added to Maude2014-04-16
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPHARMACIST
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactLINDA SERENTINO
Manufacturer Street315 ENTERPRISE DR
Manufacturer Phone6099365560
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSHUNT TUNNELER
Generic NameVALVE ACCESSORIES
Product CodeGYK
Date Received2013-12-20
Catalog Number990010
Lot Number172985
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA NEUROSCIENCES IMPLANTS S.A.
Manufacturer AddressSOPHIA ANTIPOLIS F-06921 FR F-06921


Patients

Patient NumberTreatmentOutcomeDate
10 2013-12-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.