FDAClass IIMarch 5, 2014

Optiflux F180NR High Flux Dialyzers recall

Optiflux F180NR High Flux Dialyzers; Product Number: 0500318N. Single Use acute or chronic hemanalysis treatment.

Why was Optiflux F180NR High Flux Dialyzers recalled?

Dialysate Port Leak During Priming of the Dialyzers

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Numbers: 13NU03003 13NU03010 13PU04010 13SU03001

Product
Optiflux F180NR High Flux Dialyzers; Product Number: 0500318N. Single Use acute or chronic hemanalysis treatment.
Recalling firm
Fresenius Medical Care Holdings, Inc.
Quantity
52,752 units
Distribution
Worldwide distribution: USA (nationwide) and the country of: Mexico.
Recall date
March 5, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls