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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 37 Results
Related Medical Device Recalls
 
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Product Description
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FDA Recall
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Z-0869-2025 - 8MM,TIP-UP FENESTRATED GRASPER,IS4000® REF 470347 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0860-2025 - 8MM,TENACULUM FORCEPS,IS4000® REF 470207 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0866-2025 - 8MM,SMALL GRASPING RETRACTOR,IS4000® REF 470318 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0857-2025 - 8MM,RESANO FORCEPS,IS4000 ® REF 470181 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0854-2025 - 8MM,PROGRASP FORCEPS,IS4000 ® REF 470093 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0874-2025 - 8MM,PROGRASP FORCEPS,IS4000 REF 471093 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0855-2025 - 8MM,MICRO BIPOLAR FORCEPS,IS4000 ® REF 470171 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0875-2025 - 8MM,MICRO BIPOLAR FORCEPS,IS4000 REF 471171 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0865-2025 - 8MM,MEGA SUTURECUT ND,IS4000® REF 470309 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
Z-0880-2025 - 8MM,MEGA SUTURECUT ND,IS4000 REF 471309 2 01/10/2025 FEI # 3001675293
Intuitive Surgical, Inc.
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