Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K030381 |
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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 Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula comes inside a package which is... | 2 | 06/04/2019 | Smiths Medical ASD Inc. |
Blue Line Ultra Tracheostomy Tube 8.00mm Inner Cannula REF 100/858/080 | 3 | 04/06/2006 | Smiths Medical ASD, Inc. |
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