Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K760383 |
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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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SAFSITE® Injection Sites and IV Sets manufactured with SAFSITE® Injection Sites. A device used to... | 2 | 02/18/2014 | B. Braun Medical, Inc. |
Anesthesia IV Set with Universal Spike, Backcheck Valve, two Ultrasite Injection Sites, Injection Si... | 2 | 06/05/2009 | B. Braun Medical, Inc. |
Gravity and Infusion Pump Intravenous (IV) Sets using the Y-site Ultrasite Valve including: Horizon ... | 2 | 06/12/2003 | Braun,B Medical Inc |
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