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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K962581
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FDA Recall
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Baxter Interlink System Continu-Flo Solution Set, 71" (1.8 m), 2 Injection Sites, Male Luer Lock Ada... 2 01/11/2012 Baxter Healthcare Corp.
Baxter Interlink System Continu-Flo Solution Set, 69" (1.8 m), 2 Injection Sites, Male Luer Lock Ada... 2 01/11/2012 Baxter Healthcare Corp.
Baxter Interlink System Solution Set, 67" (1.7 m), Injection Site, Male Luer Lock Adapter, Standard ... 2 01/11/2012 Baxter Healthcare Corp.
Baxter Interlink System Continu-Flo Solution Set, 71" (1.8 m), 2 Injection Sites, Male Luer Lock Ada... 2 01/11/2012 Baxter Healthcare Corp.
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