Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K080519 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PRISMAFLEX M150 SET, Product Code 109990; Dialyzer, High Permeability With Or Without Sealed Dialysa... | 2 | 02/02/2026 | VANTIVE US HEALTHCARE LLC |
| Prismaflex M Set: M150 (product code 109990). For use in providing continuous fluid management and... | 2 | 10/12/2022 | Baxter Healthcare Corporation |
| Prismaflex M150. Product number 109990. Each set is packaged in a plastic pouch, 4 pouches per carto... | 2 | 08/13/2014 | Gambro Renal Products, Incorporated |
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