VENTRICLEAR II VENTRICULAR DRAINAGE CATHETER SET WITH COOK SPECTRUM ANTIBIOTIC 50318

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other report with the FDA on 2017-04-22 for VENTRICLEAR II VENTRICULAR DRAINAGE CATHETER SET WITH COOK SPECTRUM ANTIBIOTIC 50318 manufactured by Medtronic Neurosurgery.

Event Text Entries

[73453919] The product was unavailable for return as it was discarded at the facility. Therefore an evaluation of the device performance was not possible. A good faith effort will be made to obtain the applicable information relevant to the report. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[73453920] It was reported to medtronic neurosurgery that a physician stated the catheter broke off during a procedure during insertion. According to the report, the catheter popped off/snapped while in the patient during the procedure. Reportedly, the patient experienced pneumocephalus. Per the surgeon, the current status of the patient was fine and they had returned to baseline.
Patient Sequence No: 1, Text Type: D, B5


[76206160] Additional information received reported that due to the catheter breaking, the surgeon was delayed in relieving the intracranial pressure of the brain and the patient developed pneumocephalus. According to the report, a different manufacturer? S catheter was used. It was noted that some breakage happened after the catheter had been sutured in the ventricles of the patient? S brain.
Patient Sequence No: 1, Text Type: N, H10


[78165097] Additional information received reported that no unintended section of the catheter remained inside of the patient's body and no additional procedures were required due to the reported event. This reported event is 1 of 3 similar events. Please refer to manufacturer reports #2021898-2017-00222 and #2021898-2017-00223 for details regarding the other two events. A good faith effort will be made to obtain the applicable information relevant to the report. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[94229231] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2021898-2017-00224
MDR Report Key6514826
Report SourceHEALTH PROFESSIONAL,OTHER
Date Received2017-04-22
Date of Report2017-03-23
Date of Event2017-03-17
Date Mfgr Received2017-05-22
Date Added to Maude2017-04-22
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 FDA3
Event Location3
Manufacturer ContactSTACY RUEMPING
Manufacturer Street7000 CENTRAL AVENUE NE RCW215
Manufacturer CityMINNEAPOLIS,MN CA 55432
Manufacturer CountryUS
Manufacturer Postal55432
Manufacturer Phone7635260594
Manufacturer G1MEDTRONIC NEUROSURGERY
Manufacturer Street125 CREMONA DRIVE
Manufacturer CityGOLETA CA 93117
Manufacturer CountryUS
Manufacturer Postal Code93117
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVENTRICLEAR II VENTRICULAR DRAINAGE CATHETER SET WITH COOK SPECTRUM ANTIBIOTIC
Generic NameCATHETER, VENTRICULAR (CONTAINING ANTIBIOTIC OR ANTIMICROBIAL AGENTS)
Product CodeNHC
Date Received2017-04-22
Catalog Number50318
Lot Number7025160
Device Expiration Date2018-05-18
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC NEUROSURGERY
Manufacturer Address125 CREMONA DRIVE GOLETA CA 93117 US 93117


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-04-22

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