Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1960-2020 — da Vinci Xi Surgical System

U.S. FDA — Device Enforcement · United States · 2018-11-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1960-2020
Date of alert
2018-11-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Intuitive Surgical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00886874114216
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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