ARROW CONTINUOUS NERVE BLOCK KIT FB-19604-K

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2015-03-19 for ARROW CONTINUOUS NERVE BLOCK KIT FB-19604-K manufactured by Arrow Intl., Inc..

Event Text Entries

[5590907] The customer alleges that while using the flex block kit; the catheter kinked inside the needle. No patient injury or harm reported.
Patient Sequence No: 1, Text Type: D, B5


[13107853] (b)(4). It is unknown if the device sample is available for evaluation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1036844-2015-00073
MDR Report Key4620143
Report Source06,07
Date Received2015-03-19
Date of Report2015-02-20
Date of Event2015-02-20
Date Mfgr Received2015-02-20
Date Added to Maude2015-05-01
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 ContactMARGIE BURTON, RN
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194334965
Manufacturer G1ARROW INTL., INC.
Manufacturer Street312 COMMERCE PL.
Manufacturer CityASHEBORO NC 27203
Manufacturer CountryUS
Manufacturer Postal Code27203
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARROW CONTINUOUS NERVE BLOCK KIT
Generic NameANESTHESIA CONDUCTION KIT
Product CodeOGJ
Date Received2015-03-19
Catalog NumberFB-19604-K
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARROW INTL., INC.
Manufacturer AddressREADING PA US


Patients

Patient NumberTreatmentOutcomeDate
10 2015-03-19

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