Medical Device Recalls
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1 result found
510(K) Number: K962472 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Recta... | 2 | 04/12/2018 | Teleflex Medical Europe Ltd |
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