BANDER URETERAL DIVERSION STENT SET 025706-S1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2018-07-03 for BANDER URETERAL DIVERSION STENT SET 025706-S1 manufactured by Cook Inc.

Event Text Entries

[113192438] (b)(4). Pma/510(k) #: pre-amendment. The event is currently under investigation. A follow-up report will be submitted upon receipt of additional information or completion of the investigation.
Patient Sequence No: 1, Text Type: N, H10


[113192439] When the device arrived at the hospital, it was noted that there was an unidentified foreign matter sealed inside the sterile pouch. Therefore, it was replaced with another 025706-s1. This product was not used on a patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1820334-2018-01982
MDR Report Key7659397
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2018-07-03
Date of Report2018-08-01
Date of Event2018-06-19
Date Mfgr Received2018-08-24
Device Manufacturer Date2018-04-05
Date Added to Maude2018-07-03
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 NameBANDER URETERAL DIVERSION STENT SET
Generic NameGBL CATHETER, URETERAL, GENERAL & PLASTIC SURGERY
Product CodeGBL
Date Received2018-07-03
Returned To Mfg2018-07-09
Catalog Number025706-S1
Lot Number8754583
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
10 2018-07-03

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