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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K050369
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Product Description
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FDA Recall
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Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Mon... 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.
Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle D... 2 03/30/2026 FEI # 3001675293
Intuitive Surgical, Inc.
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.
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