INTERLINK MICRO-VOLUME EXTENSION SET 1C8740

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2020-02-20 for INTERLINK MICRO-VOLUME EXTENSION SET 1C8740 manufactured by Baxter Healthcare Corporation.

Event Text Entries

[180316569] Should additional relevant information become available, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[180316570] It was reported that an unspecified quantity of interlink system non-dehp minivolume extension sets were leaking from a hole in the filter. The leaks were observed a few hours later after the patient was connected for therapy. This issue was not observed during priming. There was no report of patient injury or medical intervention associated with this event. No additional information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1416980-2020-00849
MDR Report Key9734936
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2020-02-20
Date of Report2020-03-25
Date Mfgr Received2020-03-18
Device Manufacturer Date2019-10-30
Date Added to Maude2020-02-20
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 Street25212 W. ILLINOIS ROUTE 120
Manufacturer CityROUND LAKE IL 60073
Manufacturer CountryUS
Manufacturer Postal60073
Manufacturer Phone2242702068
Manufacturer G1BAXTER HEALTHCARE - DOMINICAN REPUBLIC
Manufacturer StreetCARRETERA SANCHEZ KM 18.5 PARQUE INDUSTRIAL ITABO, PIISA
Manufacturer CityHAINA, SAN CRISTOBAL
Manufacturer CountryDR
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINTERLINK MICRO-VOLUME EXTENSION SET
Generic NameFILTER, INFUSION LINE
Product CodeFPB
Date Received2020-02-20
Model NumberNA
Catalog Number1C8740
Lot NumberDR19J29065
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE CORPORATION
Manufacturer AddressDEERFIELD IL


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-20

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