DAVOL? FEMALE CATH KIT 0035720

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other,user facility report with the FDA on 2018-12-21 for DAVOL? FEMALE CATH KIT 0035720 manufactured by C.r. Bard, Inc. (covington) -1018233.

Event Text Entries

[131161437] The investigation is still in progress. Once the investigation is complete a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10


[131161438] It was reported that the gloves inside of the female catheter kit were not wrapped up in paper like they usually are, which caused the gloves to fall out of the tray onto a non-sterile surface once the tray was opened. Allegedly, this issue caused there to be catheter associated infections. There was no information available regarding the specific treatment provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018233-2018-06138
MDR Report Key8189542
Report SourceOTHER,USER FACILITY
Date Received2018-12-21
Date of Report2019-02-04
Date Mfgr Received2019-01-16
Device Manufacturer Date2018-08-04
Date Added to Maude2018-12-21
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 ContactYONIC ANDERSON
Manufacturer Street8195 INDUSTRIAL BLVD
Manufacturer CityCOVINGTON GA 30014
Manufacturer CountryUS
Manufacturer Postal30014
Manufacturer Phone7707846100
Manufacturer G1C.R. BARD, INC. (COVINGTON) -1018233
Manufacturer Street8195 INDUSTRIAL BLVD
Manufacturer CityCOVINGTON GA 30014
Manufacturer CountryUS
Manufacturer Postal Code30014
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDAVOL? FEMALE CATH KIT
Generic NameFEMALE CATHETER KIT
Product CodeFFH
Date Received2018-12-21
Catalog Number0035720
Lot NumberNGCU3528
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerC.R. BARD, INC. (COVINGTON) -1018233
Manufacturer Address8195 INDUSTRIAL BLVD COVINGTON GA 30014 US 30014


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-12-21

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