Medical Device Recalls
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1 result found
510(K) Number: K202571 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) &... | 2 | 01/15/2026 | Intuitive Surgical, Inc. |
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