Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K141952 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instrume... | 2 | 05/21/2015 |
FEI # 1527736 Ethicon Endo-Surgery Inc |
| Endopath Echelon Vascular White Reload for Advanced Placement Tip (35mm, 4 row); Product code VASECR... | 1 | 05/20/2025 |
FEI # 1527736 Ethicon Endo-Surgery Inc |
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