The FDA announced on July 26, 2019, that Intuitive Surgical, Inc. is recalling 52 da Vinci X Surgical Systems due to potentially defective capacitors. The hazard involves vision loss or non-recoverable errors preventing system use.
How to tell if you have it
- Brand: Intuitive Surgical
- Product: da Vinci X Surgical System
- Model: IS4200
- UPC: 00886874114216
The hazard
The firm became aware of potentially defective capacitors on circuit boards installed on certain da Vinci Xi, X and SP system Vision Side Carts (VSC) and/or Patient Side Carts (PSC). As a result, users may experience vision loss or non-recoverable errors 307 or 319, preventing further use of the system.
Context
GovInfoNow's records show Intuitive Surgical, Inc. has 53 other recalls on record since June 1, 2017. Other recent recalls of similar products include Da Vinci 5 dV5 Tower NIR Handheld Camera Recall (April 24, 2026), Intuitive Surgical Da Vinci Surgical System Recall (April 22, 2026), and Da Vinci X and Xi Surgical Systems Recall (April 2, 2026). Other recent recalls of similar products include Steris ALYON Surgical Lighting System Recall (May 15, 2026), Vortex Surgical TID Pharos Illuminated Depressor Recall (December 16, 2025), and Covidien V-Loc 90 Wound Closure Device Recall (June 24, 2026).