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

Recall Z-1209-2022 — VESSEL SEALER EXTEND, Single-Use Instrument EndoWrist Instruments 8mm, da Vinci X' da Vinci Xi', REF 480422

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-1209-2022
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)
00886874115664
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.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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