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

Recall Z-2441-2019 — Fujifilm FDR Go Plus mobile X-ray system

U.S. FDA — Device Enforcement · United States · 2019-07-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2441-2019
Date of alert
2019-07-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Fujifilm Medical Systems U.S.A., Inc.
Product category
device
Product type
Devices
Reported risk: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.