NIAGARA SLIM-CATH DIALYSIS CATHETER KIT 12F X 20CM (STRAIGHT) (SHORT-TERM) (DUAL N/A 5553200

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-01-14 for NIAGARA SLIM-CATH DIALYSIS CATHETER KIT 12F X 20CM (STRAIGHT) (SHORT-TERM) (DUAL N/A 5553200 manufactured by Bard Access Systems.

Event Text Entries

[183765723] The device has not been returned to the manufacturer for evaluation. A lot history review (lhr) of recx3126 showed no other similar product complaint(s) from this lot number.
Patient Sequence No: 1, Text Type: N, H10


[183765724] It was reported that the tube sealing was broken. No other information was provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006260740-2020-00077
MDR Report Key9588746
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-01-14
Date of Report2020-01-14
Date of Event2019-12-02
Date Mfgr Received2019-12-26
Device Manufacturer Date2018-10-01
Date Added to Maude2020-01-14
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 ContactKELSEY ERICKSON
Manufacturer Street605 N. 5600 W.
Manufacturer CitySALT LAKE CITY UT 84116
Manufacturer CountryUS
Manufacturer Postal84116
Manufacturer Phone8015225937
Manufacturer G1BARD REYNOSA S.A. DE C.V. -9617592
Manufacturer StreetBLVD. MONTEBELLO #1 PARQUE INDUSTRIAL COLONIAL
Manufacturer CityREYNOSA, TAMAULIPAS
Manufacturer CountryMX
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNIAGARA SLIM-CATH DIALYSIS CATHETER KIT 12F X 20CM (STRAIGHT) (SHORT-TERM) (DUAL
Generic NameCATHETER, HEMODIALYSIS, NON-IMPLANTED
Product CodeMPB
Date Received2020-01-14
Model NumberN/A
Catalog Number5553200
Lot NumberRECX3126
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBARD ACCESS SYSTEMS
Manufacturer Address605 N. 5600 W. SALT LAKE CITY UT 84116 US 84116


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-14

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