Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K153158 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, three CLEARLINK Luer Activ... | 2 | 10/16/2025 | Baxter Healthcare Corporation |
| CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, two CLEARLINK Luer Activat... | 2 | 10/16/2025 | Baxter Healthcare Corporation |
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