Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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| Z-1732-2019 - Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula comes inside a package which is labeled in part, Product Usage: The Portex Blue Line Ultra® Tracheostomy Tubes are indicated f... | 2 | 06/04/2019 |
FEI # 3012307300 Smiths Medical ASD Inc. |
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