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

DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi', Single Use Instrument 8mm, REF 480440 — recall Z-1210-2022

U.S. FDA — Device Enforcement · United States · 2022-03-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1210-2022
Date of alert
2022-03-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Intuitive Surgical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00886874117309
Reported risk: Placing excessive tissue in the instrument jaws of the devices prior to sealing and transection can result in an insufficient seal.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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