Incident · Recall
Intuitive recalls da Vinci 8mm Maryland Bipolar Forceps over a cautery plug insert that can dislodge
Intuitive recalled the da Vinci 8mm Maryland Bipolar Forceps (REF 400172-08) because the cautery plug insert could dislodge and prevent proper connection. Distinct from the same-day Hot Shears burn recall already recorded. 697 units. Source: FDA Class 2 device recall Z-1432-2013, openFDA enforcement / accessdata.fda.gov.
Occurred 2013-05-08 · 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
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- primary-fda-database
- FDA database
The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.
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Canonical ID 02b82a36-8237-4627-98b3-aa40dabbe688