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

Recall Z-3188-2018 — sterEOS workstation

U.S. FDA — Device Enforcement · France · 2018-08-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3188-2018
Date of alert
2018-08-01
Country / jurisdiction
France
Risk level
Class II
Risk type
recall
Brand
EOS Imaging
Product category
device
Product type
Devices
Reported risk: 3D projections may be incorrect when the pair of images used is a secondary capture generated from a series containing more than two images, where one of the images has been manually flipped. Projection errors may lead to errors in calculation of 3D clinical parameters when adjusting the position, size and shape of the 3D objects used. Incorrect clinical parameters can be a contributing factor in incorrect clinical decisions, or sub-optimal surgical interventions.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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