Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K932841 |
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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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Smiths Medical, Deltec: REF 21-8011-24 Port-A-Cath Dual-Lumen. Titanium Venous Access System. RE... | 2 | 09/23/2013 | Smiths Medical ASD, Inc. |
Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray con... | 2 | 04/27/2006 | Smiths Medical MD, Inc. |
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