FDA Calls Class II Recall for da Vinci’s Newest Problem

Intuitive Surgical, manufacturer of da Vinci surgical system, informs the Food and Drug Administration (FDA) about their product’s latest problem. Intuitive disclosed that the robotic arm could stall while in use, making patients at high risk of experiencing injuries during surgery, according to an online source. In return, the FDA issued a class II recall on December 3 but not asking to remove the product from the market.  The FDA, however, warned that it could be temporarily or medical reversible health issues.
 
Before using da Vinci system, the company advised the hospitals, surgeons, and medical staff to check the device first to avoid problems.

READ MORE: Intuitive Surgical Admits to New Problem With da Vinci Surgical Robot

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