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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 274 Results
Firm: Intuitive
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Product Description
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Recall
Class
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FDA Recall
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8MM,ATRIAL RETRACTOR SHORT RIGHT,IS4000® REF 470246 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,DUAL BLADE RETRACTOR,IS4000® REF 470249 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,LARGE SUTURECUT NEEDLE DRIVER,IS4000® REF 470296 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,MEGA SUTURECUT ND,IS4000® REF 470309 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,SMALL GRASPING RETRACTOR,IS4000® REF 470318 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,MEDIUM-LARGE CLIP APPLIER,IS4000® REF 470327 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,CURVED BIPOLAR DISSECTOR,IS4000® REF 470344 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,TIP-UP FENESTRATED GRASPER,IS4000® REF 470347 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,HORIZON SMALL CLIP APPLIER,IS4000® REF 470401 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,FORCE BIPOLAR,IS4000 REF 470405 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
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