Regulatory filing
Z-1232-2026 (us_fda)
Recall of da Vinci X/Xi/5 over a software error that let instrument arms continue after failing a boot-up diagnostic; 2025.
fda recall · recalled · decided 2026-02-02
Machine-readable surfaces
- Markdown mirror: /regulatory-filings/fda-recall-davinci-instrument-arm-diagnostic-2026.md
- JSON-LD: embedded in this page’s head
- REST API: /v1/filings/7d253b17-cc5d-4ea8-ae61-874365e0fef2
- Revision history: /regulatory-filings/fda-recall-davinci-instrument-arm-diagnostic-2026/history
- Data documentation: /data
Key facts
- Jurisdiction
- us_fda
- Filing type
- fda recall
- Status
- recalled
- Filing number
- Z-1232-2026
- Decision date
- 2026-02-02
- Verification posture
- verified
- Cap-flag notes
- Slug corrected 2025 -> 2026: FDA recall Z-1232-2026 posted 2026-02-02 (primary-source-anchored). Old path 301-redirected by Rover.
Applicant
Covered models (1)
Sources (1)
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Identity
7d253b17-cc5d-4ea8-ae61-874365e0fef2