2-L HUB CONNECT ASSY REPLACEMENT SET CAR-03200

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2012-08-13 for 2-L HUB CONNECT ASSY REPLACEMENT SET CAR-03200 manufactured by Arrow Intl., Inc..

Event Text Entries

[21024417] It was reported that in the theatre on the onset of dialysis, the red hub on the pigtail of the catheter that was placed in the patient's right subclavian was found cracked and as a result, the patient suffering from kidney failure could not be dialyzed. A repair kit was used to alleviate the issue and successful dialysis was completed. A delay was reported, however, there was no additional harm to the patient due to this delay or as a result of this occurrence.
Patient Sequence No: 1, Text Type: D, B5


[21308971] (b)(4). Follow-up report will be filed if additional information becomes available.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1036844-2012-00217
MDR Report Key2698985
Report Source01,07
Date Received2012-08-13
Date of Report2012-08-13
Date of Event2012-08-02
Date Mfgr Received2012-08-02
Device Manufacturer Date2011-03-01
Date Added to Maude2012-08-20
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 FDA0
Event Location0
Manufacturer Street2400 BERNVILLE RD.
Manufacturer CityREADING PA 19605
Manufacturer CountryUS
Manufacturer Postal19605
Manufacturer Phone6103780131
Manufacturer G1ARROW INTL., INC.
Manufacturer Street312 COMMERCE PL.
Manufacturer CityASHEBORO NC 27203
Manufacturer CountryUS
Manufacturer Postal Code27203
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand Name2-L HUB CONNECT ASSY REPLACEMENT SET
Generic NameCHRONIC HEMODIALYSIS CATHETER PRODUCTS
Product CodeNFK
Date Received2012-08-13
Catalog NumberCAR-03200
Lot NumberRF1034639
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerARROW INTL., INC.
Manufacturer Address2400 BERNVILLE RD. READING PA 19605 US 19605


Patients

Patient NumberTreatmentOutcomeDate
10 2012-08-13

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