SPECTRUM VENTRICLEAR? DRAINAGE CATHETER SET N-VVDC-01-ABRM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-16 for SPECTRUM VENTRICLEAR? DRAINAGE CATHETER SET N-VVDC-01-ABRM manufactured by Cook Inc.

Event Text Entries

[130890246] This mdr is being filed after the associated complaint was reviewed under remediation protocol (b)(4), complaint/mdr retrospective review and remediation and reassessed as reportable. Additional complaint investigation and record remediation was not performed.
Patient Sequence No: 1, Text Type: N, H10


[130890247] The complainant reported that the spectrum ventricular drainage catheter was placed as a part of an external drain on (b)(6) 2016 and after three days when it was removed from the patient, a tear was found. There were no adverse effects reported due to the event and no report of an additional procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1820334-2018-03819
MDR Report Key8167855
Date Received2018-12-16
Date of Report2018-12-16
Date of Event2016-01-24
Date Mfgr Received2018-12-13
Date Added to Maude2018-12-16
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 ContactMR. LARRY POOL
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal47404
Manufacturer Phone8128294891
Manufacturer G1COOK INC
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal Code47404
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSPECTRUM VENTRICLEAR? DRAINAGE CATHETER SET
Generic NameNHC CATHETER, VENTRICULAR (CONTAINING ANTIBIOTIC 0R ANTIMICROBIAL AGENTS)
Product CodeNHC
Date Received2018-12-16
Model NumberNA
Catalog NumberN-VVDC-01-ABRM
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOOK INC
Manufacturer Address750 DANIELS WAY BLOOMINGTON IN 47404 US 47404


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-16

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