Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K932512 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Baxter Interlink System 3-Port Manifold with Check Valves, Vol. 1.0 mL, Large Bore 4-Way Stopcock Ex... | 2 | 01/11/2012 | Baxter Healthcare Corp. |
Baxter Interlink System Continu-Flo Solution Set, length 89" (2.3 m), 2 Injection Sites, Male Luer L... | 2 | 01/11/2012 | Baxter Healthcare Corp. |
Baxter Interlink System Continu-Flo Solution Set, length 89" (2.3 m), 2 Injection Sites, Male Luer L... | 2 | 01/11/2012 | Baxter Healthcare Corp. |
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