Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K830730 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PORT-A-CATH Plastic Hub Needles, 0.9mm (20G) x 19mm (3/4 in.) 90-degree. REF 21-2287-24 The Plas... | 2 | 10/21/2015 |
FEI # 2183502 Smiths Medical ASD, Inc. |
| Port-A-Cath Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr In... | 2 | 07/20/2004 |
FEI # 2183502 Deltec, Inc |
| Port-A-Cath Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr In... | 2 | 07/20/2004 |
FEI # 2183502 Deltec, Inc |
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