ALGOLINE CATHETER KIT, CLOSED TIP CATHETER 81102

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2001-11-05 for ALGOLINE CATHETER KIT, CLOSED TIP CATHETER 81102 manufactured by Medtronic Neurosurgery.

Event Text Entries

[18336054] The algoline catheter came in defective. There was a hole in the catheter.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2021898-2001-00110
MDR Report Key361567
Report Source06
Date Received2001-11-05
Date of Report2001-10-05
Date of Event2001-10-05
Date Facility Aware2001-10-05
Date Mfgr Received2001-10-05
Device Manufacturer Date1998-04-01
Date Added to Maude2001-11-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJEFFREY HENDERSON
Manufacturer Street125 CREMONA DRIVE
Manufacturer CityGOLETA CA 931175500
Manufacturer CountryUS
Manufacturer Postal931175500
Manufacturer Phone8059681546
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameALGOLINE CATHETER KIT, CLOSED TIP CATHETER
Generic NameANALGESIA CONDUCTION CATHETER, SHORT TERM
Product CodeMAJ
Date Received2001-11-05
Returned To Mfg2001-10-29
Model NumberNA
Catalog Number81102
Lot NumberL6912
ID NumberNA
Device Expiration Date2003-04-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age3.5 YR
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key350723
ManufacturerMEDTRONIC NEUROSURGERY
Manufacturer Address125 CREMONA DRIVE GOLETA CA 931175500 US
Baseline Brand NameALGOLINE CATHETER KIT, CLOSED TIP CATHETER
Baseline Generic NameCATHETER, PERCUTANEOUS, INTRASPINAL, SHORT-TERM
Baseline Model NoNA
Baseline Catalog No81102
Baseline IDNA
Baseline Device FamilyALGOLINE
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]60
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK911382
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 2001-11-05

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