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

Recall Z-2306-2018 — Artis Q.zeego, Material no. 10848283, for angiography and whole body radiographic/fluoroscopic procedures.

U.S. FDA — Device Enforcement · United States · 2018-05-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2306-2018
Date of alert
2018-05-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10848283
Reported risk: After the Large Display returns from power save mode, it may not show an image, and stay black without showing an error message although X-ray is still possible. The problem does not occur during an ongoing procedure. If the problem occurs, the system cannot be operated normally. It may be necessary to cancel or restart the treatment or transfer the patient to an alternate or another system.
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.