Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K201867 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Automated Peritoneal Dialysis System. Used for automatic control of dialysis solution exchanges. | 2 | 04/01/2023 | Baxter Healthcare Corporation |
| Sharesource Connectivity Platform for Use with Homechoice Claria Product Code 5CGM01 software ve... | 2 | 10/29/2025 | Vantive US Healthcare LLC |
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