Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K150679 |
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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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EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into th... | 2 | 04/11/2024 | Boston Scientific Corporation |
EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the ... | 2 | 04/11/2024 | Boston Scientific Corporation |
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