BARD? WOVEN URETERAL CATHETER 036106

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-05-26 for BARD? WOVEN URETERAL CATHETER 036106 manufactured by C.r. Bard, Inc. (gfo) -1313046.

Event Text Entries

[76238402] The investigation is still in progress. Once the investigation is complete a supplemental report will be filed. The information provided by bard represents all of the known information at this time. Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bard. The device was not returned.
Patient Sequence No: 1, Text Type: N, H10


[76238403] It was reported that the catheter was missing from the packaging. The complainant stated that the packaging was sealed , when it was noted that no catheter was inside. No patient involvement was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018233-2017-02753
MDR Report Key6595510
Date Received2017-05-26
Date of Report2017-06-24
Date Mfgr Received2017-06-12
Device Manufacturer Date2015-08-10
Date Added to Maude2017-05-26
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 ContactAMY GRAVLEY
Manufacturer Street8195 INDUSTRIAL BLVD
Manufacturer CityCOVINGTON GA 30014
Manufacturer CountryUS
Manufacturer Postal30014
Manufacturer Phone7707846100
Manufacturer G1C.R. BARD, INC. (GFO) -1313046
Manufacturer Street289 BAY ROAD
Manufacturer CityQUEENSBURY NY 12804
Manufacturer CountryUS
Manufacturer Postal Code12804
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBARD? WOVEN URETERAL CATHETER
Generic NameURETHRAL CATHETER
Product CodeEYB
Date Received2017-05-26
Catalog Number036106
Lot NumberGFZE2448
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerC.R. BARD, INC. (GFO) -1313046
Manufacturer Address289 BAY ROAD QUEENSBURY NY 12804 US 12804


Patients

Patient NumberTreatmentOutcomeDate
10 2017-05-26

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