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

Recall Z-2560-2019 — Monaco RTP System, 5.40 Unity, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment plans and displays, on-sc

U.S. FDA — Device Enforcement · United States · 2019-09-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2560-2019
Date of alert
2019-09-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Elekta Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00858164002190
Reported risk: It is possible that the forced electron density settings will be changed for some structures unintentionally and this can result in incorrect dose calculation.
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.