VENTRICLEAR DRAINAGE CATHETER SET N/A 50318

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2018-03-22 for VENTRICLEAR DRAINAGE CATHETER SET N/A 50318 manufactured by Cook Inc.

Event Text Entries

[103298044] (b)(4). This report includes information known at this time. A follow up report will be submitted should additional relevant information become available.
Patient Sequence No: 1, Text Type: N, H10


[103298045] It was reported that the health care provider (hcp) attempted to use the catheter but found that it was defective as there was a hole in the side of it. The hcp was unable to use the device. There was no known impact or consequence to the patient. Additional information has been requested but was not provided the reporter.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1820334-2018-00425
MDR Report Key7364357
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2018-03-22
Date of Report2018-06-22
Date of Event2018-02-24
Date Mfgr Received2018-02-28
Device Manufacturer Date2017-07-13
Date Added to Maude2018-03-22
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 ContactMR. LARRY POOL
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal47404
Manufacturer Phone8123392235
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 Report3

Device Details

Brand NameVENTRICLEAR DRAINAGE CATHETER SET
Generic NameNHC CATHETER, VENTRICULAR (CONTAINING ANTIBIOTIC 0R ANTIMICROBIAL AGENTS)
Product CodeNHC
Date Received2018-03-22
Model NumberN/A
Catalog Number50318
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
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 2018-03-22

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