FDANovember 21, 2018device

da Vinci X Surgical System

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

The hazard

Due to a manufacturing variation in the arm that can result in a persistent recoverable fault error (error 23087) and loss of arm functionality prior or during surgery.

What to do

FDA enforcement status: Terminated

Brands named

intuitive surgicalintuitive

UPCs

00886874114216

Recall history

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

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