Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K003498 |
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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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Fresenius Optiflux F160NRe Hemodialyzer Catalog number: 0500316E Intended for patients with acut... | 2 | 03/30/2012 | Fresenius Medical Care Holdings, Inc. |
Optiflux F200A High Flux Dialyzers; Product Number: 0500320A. Single Use acute or chronic hemanal... | 2 | 02/26/2014 | Fresenius Medical Care Holdings, Inc. |
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