Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K002761 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Optiflux F200NRe High Flux Dialyzers; Product Number: 0500320E. Single Use acute or chronic heman... | 2 | 02/26/2014 | Fresenius Medical Care Holdings, Inc. |
Optiflux F160NRe High Flux Dialyzers; Product Number: 0500316E. Single Use acute or chronic heman... | 2 | 02/26/2014 | Fresenius Medical Care Holdings, Inc. |
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