DAVOL? INFANT CATH KIT 0035630

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-11-27 for DAVOL? INFANT CATH KIT 0035630 manufactured by C.r. Bard, Inc. (covington) -1018233.

Event Text Entries

[128560550] The investigation is still in progress. Once the investigation is complete a supplemental report will be filed. The device was not returned.
Patient Sequence No: 1, Text Type: N, H10


[128560551] It was reported that two infant catheter kits were sent, received and used on one infant without the povidone-iodine included. Reportedly, as a result, the infant contracted a urinary tract infection. The uti was treated with antibiotics. It was noted that the yellow label indicating the absence of the povidone-iodine was adhered to the packaging. However, the nurse did not notice the label upon first looking at the package.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018233-2018-05642
MDR Report Key8108877
Date Received2018-11-27
Date of Report2019-01-18
Date Mfgr Received2019-01-02
Device Manufacturer Date2018-05-23
Date Added to Maude2018-11-27
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 Report0

Device Details

Brand NameDAVOL? INFANT CATH KIT
Generic NameINFANT CATHETER KIT
Product CodeFFH
Date Received2018-11-27
Catalog Number0035630
Lot NumberNGCS1862
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. Required No Informationntervention 2018-11-27

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