WITTICH NITINOL STONE BASKET N/A WNSB-12-24

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-05-23 for WITTICH NITINOL STONE BASKET N/A WNSB-12-24 manufactured by Cook Inc.

Event Text Entries

[145904974] (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


[145904975] It was reported a wittich nitinol stone basket was selected to remove a biliary stone following percutaneous biliary drainage. After the device secured the stone, it was pulled towards the sheath. Per the initial report, "the product was disconnected while pulling the basket". Additional intervention was required to recover the separated parts. No other adverse effects were reported for this incident.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1820334-2019-01184
MDR Report Key8635514
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-05-23
Date of Report2019-08-12
Date of Event2019-05-14
Date Mfgr Received2019-08-07
Date Added to Maude2019-05-23
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 NameWITTICH NITINOL STONE BASKET
Generic NameLQR DISLODGER, STONE BILIARY
Product CodeLQR
Date Received2019-05-23
Returned To Mfg2019-06-13
Model NumberN/A
Catalog NumberWNSB-12-24
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCOOK INC
Manufacturer Address750 DANIELS WAY BLOOMINGTON IN 47404 US 47404


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-05-23

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