ARROW MULTI-LUMEN/PSI SET SI-11142

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2020-03-24 for ARROW MULTI-LUMEN/PSI SET SI-11142 manufactured by Arrow International Inc..

Event Text Entries

[184818237] Qn#: (b)(4). Potential lot#: 71f18c0280.
Patient Sequence No: 1, Text Type: N, H10


[184818238] The customer reports that the head of the dilator was torn. The doctor used a new product and completed the procedure without incident.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006425876-2020-00260
MDR Report Key9871944
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2020-03-24
Date of Report2020-03-11
Date of Event2019-12-28
Date Mfgr Received2020-03-11
Date Added to Maude2020-03-24
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 ContactMARGIE BURTON, RN
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194334965
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 NameARROW MULTI-LUMEN/PSI SET
Generic NameCATHETER,INTRAVASCULAR,THERAP
Product CodeFOZ
Date Received2020-03-24
Catalog NumberSI-11142
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARROW INTERNATIONAL INC.
Manufacturer AddressREADING PA


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-24

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