Class II recall of da Vinci reusable instruments (forceps, scissors, drivers, graspers) over cable fraying
S3 · not documented · Intuitive Surgical
Record
| Company | Intuitive Surgical |
| Industry | Medical robotics |
| Type(s) | recall |
| Date | not documented (date not documented) |
| Time of day | not documented |
| Location | no physical site (recall / fleet-wide / aggregate record) |
| Severity | (recall, enforcement, or fleet-wide fault) |
| Scale | multiple instrument models, US and international distribution |
| Confidence | medium |
| Verified flag | Cited source on file; not independently re-verified |
Summary
Intuitive Surgical initiated FDA Class II recalls of multiple reusable da Vinci instrument types after an increase in complaints about frayed or broken internal cables causing instrument malfunction during procedures.
Primary source
Publisher: MedTech Dive · Retrieved: 2026-09-16
Supporting source rows (1)
| Date | Supporting source row | Publisher | Link |
|---|---|---|---|
| not documented | Class II recall of da Vinci reusable instruments (forceps, scissors, drivers, graspers) over cable fraying | MedTech Dive | MedTech Dive |
Intuitive Surgical other incidents timeline
Medical robotics context
recall context
Intuitive Surgical industry position
Related incidents
Other Intuitive Surgical entries
- 18 Mar 2026 - FDA issues emergency alert on da Vinci-compatible surgical stapler reloads after 1 death, 4 injuries
- 11 Mar 2026 - Class I recall of da Vinci SureForm stapler reloads after patient death
- 26 Feb 2025 - Class II recall of da Vinci 5 foot pedal over spring failure
- ~2025 - 2015-2025 MAUDE study finds continued adverse event rate in da Vinci procedures
- ~Sep 2021 - Lawsuit: da Vinci surgical robot burned woman's small intestine
- ~2013 - 14-year FDA MAUDE analysis finds 144 deaths, 1,391 injuries in robotic surgery (2000-2013)
- not documented - NBC News 10-year MAUDE analysis of da Vinci adverse events
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