OPTIFLUX F18NRE DIALYZER FINISHED ASSY 0500308E

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-11-19 for OPTIFLUX F18NRE DIALYZER FINISHED ASSY 0500308E manufactured by Ogden Manufacturing Plant.

Event Text Entries

[127553818] The plant investigation is in process. A supplemental mdr will be submitted upon completion of this activity.?
Patient Sequence No: 1, Text Type: N, H10


[127553819] A user facility reported a dialyzer blood leak from a fresenius optiflux f18nre dialyzer that occurred during patient treatment. The blood leak was observed 5 minutes after the start of treatment. The dialyzer and bloodlines were replaced, and the patient completed treatment on the same fresenius 4008s machine with no injury, adverse event, or medical intervention. The dialyzer was discarded and was not available for return.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1713747-2018-00458
MDR Report Key8083904
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-11-19
Date of Report2018-12-10
Date of Event2018-11-02
Date Mfgr Received2018-12-07
Device Manufacturer Date2018-02-05
Date Added to Maude2018-11-19
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 ContactTHOMAS C. JOHNSON
Manufacturer Street920 WINTER ST.
Manufacturer CityWALTHAM MA 02451
Manufacturer CountryUS
Manufacturer Postal02451
Manufacturer Phone7816999499
Manufacturer G1OGDEN MANUFACTURING PLANT
Manufacturer Street475 WEST 13TH STREET
Manufacturer CityOGDEN UT 84404
Manufacturer CountryUS
Manufacturer Postal Code84404
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOPTIFLUX F18NRE DIALYZER FINISHED ASSY
Generic NameDIALYZER, CAPILLARY, HOLLOW FIBER
Product CodeFJI
Date Received2018-11-19
Catalog Number0500308E
Lot Number18BU01002
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeMO
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOGDEN MANUFACTURING PLANT
Manufacturer Address475 WEST 13TH STREET OGDEN UT 84404 US 84404


Patients

Patient NumberTreatmentOutcomeDate
10 2018-11-19

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