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

Recall Z-2388-2018 — Discovery IGS 740 Interventional Fluoroscopic X-ray Systems

U.S. FDA — Device Enforcement · France · 2018-03-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2388-2018
Date of alert
2018-03-29
Country / jurisdiction
France
Risk level
Class II
Risk type
recall
Brand
GE Medical Systems, SCS
Product category
device
Product type
Devices
Reported risk: The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in the loss of imaging mode before or during fluoroscopic use.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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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.