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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K150284
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Product Description
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Recall
Class
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FDA Recall
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8MM, ROUND TIP SCISSORS, IS4000 ® REF 470007 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,DEBAKEY FORCEPS,IS4000 ® REF 470036 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,CADIERE FORCEPS,IS4000 ® REF 470049 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,LARGE SUTURECUT NEEDLE DRIVER,IS4000 REF 471296 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,CADIERE FORCEPS,IS4000 REF 471049 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,COBRA GRASPER,IS4000 REF 471190 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
8MM,MEGA NEEDLE DRIVER,IS4000® REF 470194 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
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