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

Recall Z-1871-2014 — IS4000 da Vinci Xi - Endoscope accessory; 0 Degree, 8mm Endoscope. Intuitive Surgical Inc.

U.S. FDA — Device Enforcement · United States · 2014-06-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1871-2014
Date of alert
2014-06-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Intuitive Surgical, Inc.
Product category
device
Product type
Devices
Reported risk: In some procedures when using the endoscope in conjunction with the IS4000 (da Vinci Xi) System, the surgical view has an orange-yellow tint which can make it hard to differentiate between tissue
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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