ARROW STIMUCATH SET: 19G CATH, 17G X 8CM NDL AB-19608-S

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2014-08-19 for ARROW STIMUCATH SET: 19G CATH, 17G X 8CM NDL AB-19608-S manufactured by Arrow Intl., Inc..

Event Text Entries

[4719807] The event is reported as: the customer alleges that it is difficult to advance/remove the stylet into the cannula. The customer states that there is some resistance in the area of the grip. No report of pt injury/harm.
Patient Sequence No: 1, Text Type: D, B5


[12354077] The device sample was not returned for eval at the time of the report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1036844-2014-00340
MDR Report Key4092567
Report Source01,05,06
Date Received2014-08-19
Date of Report2014-07-28
Date of Event2014-07-28
Date Mfgr Received2014-07-28
Device Manufacturer Date2013-07-01
Date Added to Maude2014-09-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMARGIE BURTON, RN, REGULATORY AF
Manufacturer StreetPO BOX 12600
Manufacturer CityDURHAM NC 27709
Manufacturer CountryUS
Manufacturer Postal27709
Manufacturer Phone9194334965
Manufacturer G1ARROW INTL., INC.
Manufacturer Street312 COMMERCE PL.
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARROW STIMUCATH SET: 19G CATH, 17G X 8CM NDL
Generic NameNERVE BLOCK TRAY
Product CodeOGJ
Date Received2014-08-19
Catalog NumberAB-19608-S
Lot Number23F13G0669
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 2014-08-19

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.