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

Recall Z-1583-2015 — AXIOM ARISTOS FX; Multipurpose Radiography System (MPRS) is a dedicated x-ray system with a flat panel detector which allows the acquisition of x-ray exposures without the use of conventional film/screen systems. The MPRS allows radiographic exposures of the whole body including skull, spinal column

U.S. FDA — Device Enforcement · United States · 2015-04-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1583-2015
Date of alert: 2015-04-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Siemens Medical Solutions USA, Inc
Product category: device
Product type: Devices

Reported risk: If the cable cart and the corrugated hose are unable to move freely, the cable holder could drop down and hit patients or system operators.

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.

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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