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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 9 of 9 Results
510(K) Number: K961495
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Product Description
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FDA Recall
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Baxter Interlink System Huber Needle Extension Set, product code 2N3709; An Rx sterile, nonpyrogeni... 2 08/30/2005 Baxter Healthcare Corp.
Baxter Interlink System Huber Needle Extension Set, product code 2N3703; An Rx sterile, nonpyrogenic... 2 08/30/2005 Baxter Healthcare Corp.
Baxter Interlink System Huber Needle Extension Set, product code 2N3706; An Rx sterile, nonpyrogeni... 2 08/30/2005 Baxter Healthcare Corp.
Baxter Interlink System Huber Needle Extension Set, product code 2N3707; An Rx sterile, nonpyrogeni... 2 08/30/2005 Baxter Healthcare Corp.
Baxter Interlink System Huber Needle Extension Set, product code 2N3716; An Rx sterile, nonpyrogeni... 2 08/30/2005 Baxter Healthcare Corp.
Baxter Interlink System Huber Needle Extension Set, product code 2N3710; An Rx sterile, nonpyrogeni... 2 08/30/2005 Baxter Healthcare Corp.
Baxter Interlink System Huber Needle Extension Set, product code 2N3712; An Rx sterile, nonpyrogeni... 2 08/30/2005 Baxter Healthcare Corp.
Baxter Interlink System Huber Needle Extension Set, product code 2N3714; An Rx sterile, nonpyrogeni... 2 08/30/2005 Baxter Healthcare Corp.
Baxter Interlink System Huber Needle Extension Set; a sterile 10'' fluid pathway with an Interlink Y... 3 07/28/2005 Baxter Healthcare Corp.
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