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

Recall Z-2412-2024 — Surgical Image Guidance Functionality, software used with NGENUITY 3D Visualization System, Part Number: 8065000399

U.S. FDA — Device Enforcement · United States · 2024-05-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2412-2024
Date of alert
2024-05-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Alcon Research LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00380650003997
Reported risk: After surgery initiation, while using surgical image guidance, if significant eye rotation/movement occurs, a software anomaly may cause re-establishment of incorrect new registration angle, range indicator will display incorrectly, which could result in incorrect placement of toric IOL axis, which could cause astigmatic error under/over correction resulting in decreased uncorrected visual acuity.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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