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Recall Observatory FDA recall evidence

Device product

Optiflux B200 Flux Dialyzers; Product Number: 0500325E. Single Use acute or chronic hemanalysis treatment.

Z-1105-2014

February 04, 2014

Class II

Product summary

Firm
Fresenius Medical Care Holdings, Inc.
Event
Event 67313
Status
Terminated
Classification
Class II
Quantity
100,008 units
Official record key
device-enforcement:Z-1105-2014

Official wording

Reason: Dialysate Port Leak During Priming of the Dialyzers

Code information: Lot Numbers: 13LU02011 13LU02013 13NU02016 13NU02017

Distribution pattern: Worldwide distribution: USA (nationwide) and the country of: Mexico.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Dialysate Port Leak During Priming of the Dialyzers