Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K031057 |
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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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Portex Perfit Percutaneous Tracheostomy Tube Replacement Kit, Sterile Ref: 536090 | 2 | 11/07/2007 | Smiths Medical ASD, Inc. |
Portex Per-Fit Percutaneous Dilational Tracheostomy Kit, ID 8.0mm Product Number: 535080 | 2 | 06/04/2005 | Smiths Medical ASD, Inc. |
Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 9.0mm Product Number: 535090 | 2 | 06/04/2005 | Smiths Medical ASD, Inc. |
Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 8.0mm Product Number: 538080E | 2 | 06/04/2005 | Smiths Medical ASD, Inc. |
Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 9.0mm Product Number: 538090E | 2 | 06/04/2005 | Smiths Medical ASD, Inc. |
Portex Per-Fit Percutaneous Dilational Tracheostomy Kit ,ID 7.0mm Product Number: 535070 | 2 | 06/04/2005 | Smiths Medical ASD, Inc. |
Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 7.0mm Product Number: 538070E | 2 | 06/04/2005 | Smiths Medical ASD, Inc. |
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