Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K080519 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 |
-