Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K050369 |
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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| Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retr... | 2 | 03/30/2026 |
FEI # 3001675293 Intuitive Surgical, Inc. |
| Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Doubl... | 2 | 03/30/2026 |
FEI # 3001675293 Intuitive Surgical, Inc. |
| Assembly, Patient Side Manipulator on da Vinci Surgical Systems: da Vinci S Surgical System; da Vi... | 2 | 12/03/2013 |
FEI # 3001675293 Intuitive Surgical, Inc. |
| ACCESSORY BASE STARTER KIT,IS3000; Product Usage: The intended use of the Instrument arm dra... | 2 | 07/27/2012 |
FEI # 3001675293 Intuitive Surgical, Inc. |
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