Incident · Recall
Intuitive recalls da Vinci X/Xi and S/Si Clip Appliers over unexpected motion from partial disengagement
Intuitive recalled da Vinci Clip Appliers because partial disengagement could cause unexpected instrument motion during surgery. Two paired recalls: X/Xi (90,628 units) and S/Si (62,895 units). Source: FDA Class 2 device recalls Z-1460-2022 and Z-1459-2022, accessdata.fda.gov / openFDA enforcement.
Occurred 2022-07-01 · Intuitive Surgical · Investigated by FDA
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Methodology: Verified · 1 source (1 primary) · last reviewed 2026-08-09
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Last reviewed 2026-08-09
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- FDA database
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Canonical ID ddc44cc5-f97e-4558-8db7-7fad9ea9557f