EPIDURAL CATHETERIZATION SET JC-05400-B

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 2020-02-26 for EPIDURAL CATHETERIZATION SET JC-05400-B manufactured by Arrow International Inc..

Event Text Entries

[181367686] 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


[181367687] It was reported that the lor syringe was leaking the syringe had no resistance. It happened for 3 syringes in a row. The staff in the theater room opened 3 kits with syringes having the same issue. The lot was put in quarantine. Additional information indicates that there was no patient injury and the leak was air found upon opening the kit.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006425876-2020-00190
MDR Report Key9757703
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-02-26
Date of Report2020-02-12
Date of Event2020-02-12
Date Mfgr Received2020-02-12
Device Manufacturer Date2019-10-03
Date Added to Maude2020-02-26
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 ContactEFFIE JEFFERSON
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194332672
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 Received2020-02-26
Catalog NumberJC-05400-B
Lot Number71F19J2204
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARROW INTERNATIONAL INC.
Manufacturer AddressREADING PA


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-26

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