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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K203609
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Product Description
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Recall
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FDA Recall
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CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backchec... 2 10/16/2025 FEI # 1417572
Baxter Healthcare Corporation
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backch... 2 10/16/2025 FEI # 1417572
Baxter Healthcare Corporation
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backch... 2 10/16/2025 FEI # 1417572
Baxter Healthcare Corporation
Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 ... 2 09/19/2025 FEI # 1417572
Baxter Healthcare Corporation
Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519 2 01/22/2025 FEI # 1417572
Baxter Healthcare Corporation
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