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

Recall Z-0005-2015 — Siemens Luminos Agile Max system The Luminos Agile is intended to be used as a universal imaging system for radiographic and fluoroscopic studies. Using either film cassettes or a digital mobile flat detector, it can perform a range of applications including general R/F, angiography and pediatric

U.S. FDA — Device Enforcement · United States · 2014-09-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0005-2015
Date of alert
2014-09-02
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)
10762472
Reported risk: Two malfunctions posing potential risk to patients were identified with Siemens Ysio Max, AXIOM Luminos dRF Max, Uroskop Omnia Max, and Luminos Agile Max systems with a specific set of serial numbers that will cause lost images due to an automatic Radiology Information System (RIS) worklist update, thus causing examinations to be repeated. Image label may also be displayed incorrectly after images
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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