EPIDURAL CATHETERIZATION SET IPN046313 JC-05400-DCS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-02-11 for EPIDURAL CATHETERIZATION SET IPN046313 JC-05400-DCS manufactured by Arrow International Inc..

Event Text Entries

[180325522] Qn#: (b)(4). The device has not been returned for investigation. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


[180325523] It was reported that there is a lack of pressure in the lor syringe. Further information indicates that the syringe leaked liquid and around 10 patients were concerned but he is not able to provide the exact quantity. There was no patient consequence, no device available for investigation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006425876-2020-00166
MDR Report Key9695867
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-02-11
Date of Report2020-01-24
Date of Event2020-01-24
Date Mfgr Received2020-03-11
Date Added to Maude2020-02-11
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 ContactJASMINE BROWN
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9193614124
Manufacturer G1ARROW INTERNATIONAL CR, A.S.
Manufacturer StreetJAMSKA 2359/47
Manufacturer CityZDAR NAD SAZAVOU 591 01
Manufacturer CountryEZ
Manufacturer Postal Code591 01
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEPIDURAL CATHETERIZATION SET
Generic NameANESTHESIA CONDUCTION KIT
Product CodeCAZ
Date Received2020-02-11
Model NumberIPN046313
Catalog NumberJC-05400-DCS
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARROW INTERNATIONAL INC.
Manufacturer AddressREADING PA


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-11

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