FDAAugust 29, 2025device

Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX F160NRe 12/CS 1.5SA EBEAM, (2) 0500318E OPTIFLUX F180NRe 12/CS 1.7SA EBEAM, (3) 0500320E OPTIFLUX F200NRe 12/CS 1.9SA EBEAM, (4) 0500325E OPTIFLUX F250NRe 12/CS 2.5SA EBEAM

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

To provide further information to the user to ensure proper use of the medical device. the caps had been changed from a threaded version to a press-on version whereby the user must press the caps firmly onto the dialyzer to securely affix the cap.

What to do

FDA enforcement status: Ongoing

Brands named

fresenius medical carefreseniusfresenius medical

UPCs

840861100149840861100156840861100163840861100170

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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