EPIDURAL CATHETERIZATION COMPONENT EC-05500

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 2020-02-27 for EPIDURAL CATHETERIZATION COMPONENT EC-05500 manufactured by Arrow International Inc..

Event Text Entries

[181368584] 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


[181368585] It was reported that on january 10 there was a break of an epidural catheter in the back of a patient during the withdrawal lot number 71f19h1992. An x-ray was done on the patient and confirmation of the catheter tip present. Withdrawal of all catheters from the same lot; they were thrown away. The patient had a consultation in neurosurgery. After evaluation there is more risk to remove than leaving it there since it has no symptoms. The patient is fine.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006425876-2020-00196
MDR Report Key9763468
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-02-27
Date of Report2020-02-17
Date of Event2020-01-10
Date Mfgr Received2020-02-17
Device Manufacturer Date2019-08-27
Date Added to Maude2020-02-27
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 COMPONENT
Generic NameANESTHESIA CONDUCTION CATHETER
Product CodeBSO
Date Received2020-02-27
Catalog NumberEC-05500
Lot Number71F19H1992
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 2020-02-27

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