FDAApril 1, 2019device

da Vinci SP surgical system

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Intuitive has become aware that the da Vinci SP system may trigger a mechanical vibration of the instrument tips and endoscope due to a software anomaly. This issue has the potential to occur only under the following, extremely rare specific conditions: 1) the user is activating Adjust Mode, AND 2) the instrument Arm is near its vertical position limit, AND 3) the user is applying sustained force against the hand control haptic feedback.

What to do

FDA enforcement status: Terminated

Brands named

intuitive surgicalintuitive

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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