Incident · Recall
Intuitive recalls da Vinci 8mm ProGrasp Forceps over frayed or broken grip cables
Intuitive recalled da Vinci 8mm ProGrasp Forceps (REF 471093) as part of the reusable-instrument wave over frayed or broken grip cables that could cause loss of instrument control during surgery. 99,249 units. Source: FDA Class 2 device recall Z-0874-2025, openFDA enforcement (api.fda.gov/device/enforcement) / accessdata.fda.gov.
Occurred 2024-12-19 · Intuitive Surgical · Investigated by FDA
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Methodology: Verified · 1 source (1 primary) · last reviewed 2026-08-09
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Verified
High confidence
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Last reviewed 2026-08-09
Sources by quality tier
- 1
- primary-fda-database
- FDA database
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Canonical ID 79c98470-5608-4ee4-b3f2-a69712d7d73c