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

Recall Z-0169-2013 — MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR) used for oncology workflow management. It lets users supply electronic patient charts and assemble care plans, order diagnostic tests, and prescribe medications. It also lets users import, view, annotate, manipulate, enhance

U.S. FDA — Device Enforcement · United States · 2012-09-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0169-2013
Date of alert: 2012-09-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Elekta, Inc.
Product category: device
Product type: Devices

Reported risk: A patient was seriously mistreated after a user made and saved an inadvertent change to the definition of a treatment filed in MOSAIQ.

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.

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