Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K902180 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Portex Inner Cannula for Tracheostomy Tube Size 7.0 mm, REF Code 566070 | 2 | 07/20/2004 | Smiths Medical ASD, Inc |
| Portex Inner Cannula for Tracheostomy Tube, 8.0 mm, REF Code 566080 | 2 | 07/20/2004 | Smiths Medical ASD, Inc |
| Portex Tracheal Tube Guide 15 Fr, non-sterile Catalog Number: 153013 | 3 | 07/20/2004 | Smiths Medical ASD, Inc |
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