Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K180739 |
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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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| CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves. 10 drops... | 2 | 10/16/2025 | Baxter Healthcare Corporation |
| CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backch... | 2 | 10/16/2025 | Baxter Healthcare Corporation |
| CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activa... | 2 | 10/16/2025 | Baxter Healthcare Corporation |
| Baxter Solution Set with Duo-Vent Spike, REF 2R8404 | 2 | 01/22/2025 | Baxter Healthcare Corporation |
| Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538 | 2 | 01/22/2025 | Baxter Healthcare Corporation |
| CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401 | 2 | 03/14/2024 | Baxter Healthcare Corporation |
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