Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K932840 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray con... | 2 | 04/27/2006 |
FEI # 2183502 Smiths Medical MD, Inc. |
| Port-A-Cath II Polysulfone/Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm... | 2 | 07/20/2004 |
FEI # 2183502 Deltec, Inc |
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