Medical Device Recalls
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1 result found
510(K) Number: K041348 |
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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 UNLTRperc Percutaneous Dilation Tracheostomy Kit, REF 100/596/090 - Product Usage: intended f... | 2 | 07/01/2021 | Smiths Medical ASD Inc. |
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