Medical Device Recalls
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1 result found
510(K) Number: K173337 |
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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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| VESSEL SEALER EXTEND, Single-Use Instrument EndoWrist Instruments 8mm, da Vinci X' da Vinci Xi', REF... | 2 | 05/31/2022 | Intuitive Surgical, Inc. |
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