ARROW CONTINUOUS NERVE BLOCK KIT AB-20608-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 2014-08-20 for ARROW CONTINUOUS NERVE BLOCK KIT AB-20608-K manufactured by Arrow Intl., Inc..

Event Text Entries

[4900553] The event is reported as: the customer alleges that there is a hole in the catheter. The alleged defect was detected during a nerve block procedure. The pt's condition is reported as fine.
Patient Sequence No: 1, Text Type: D, B5


[12296947] The device sample was not returned for eval at the time of this report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1036844-2014-00346
MDR Report Key4062893
Report Source06,07
Date Received2014-08-20
Date of Report2014-08-05
Date of Event2014-08-01
Date Mfgr Received2014-08-05
Date Added to Maude2014-09-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMARGIE BURTON, RN
Manufacturer StreetPO BOX 12600
Manufacturer CityDURHAM NC 27709
Manufacturer CountryUS
Manufacturer Postal27709
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 NameNERVE BLOCK KIT
Product CodeOGJ
Date Received2014-08-20
Catalog NumberAB-20608-K
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARROW INTL., INC.
Manufacturer AddressREADING PA 19605 US 19605


Patients

Patient NumberTreatmentOutcomeDate
10 2014-08-20

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