Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K922749 |
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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 Tracheostomy Tube Decannulation Cap for use only with Fenestrated Tracheostomy Tubes Catalog... | 2 | 11/24/2004 | Smiths Medical ASD, Inc. |
Portex Lo-Profile Tracheostomy Tube Decannulation Cap Catalog Number: 582000 | 2 | 11/24/2004 | Smiths Medical ASD, Inc. |
Lo-Profile Fenestrated Tracheostomy Tube, Cuffed and Fenestrated Tube I.D. 9.0mm Catalog Number: 59... | 3 | 07/23/2003 | Portex Inc. |
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