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

Recall Z-2175-2014 — DX-D 600 - DXD Imaging Package Product Usage:Is indicated for use in providing diagnostic quality images to aid the physician with diagnosis. Systems can be used with MUSICA2 image processing to create radiographic images of the skeleton including skull, spinal column and extremities, check abdom

U.S. FDA — Device Enforcement · United States · 2014-07-02 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2175-2014
Date of alert: 2014-07-02
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: AGFA Healthcare Corp.
Product category: device
Product type: Devices

Reported risk: Some customers reported that while using the DX-D600 in room or exam preparation, the Overhead Tube Crane (OTC) showed increased velocity and uncontrolled longitudinal movement.

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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