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

Recall Z-1752-2019 — Proteus XR/a The Proteus XR/a radiographic system offers the flexibility to choose a configuration based upon your specific requirements. The system provides exceptional image quality, high frequency X-ray generation, easy patient positioning, intuitive operator control and minimal system mainte

U.S. FDA — Device Enforcement · United States · 2019-03-29 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1752-2019
Date of alert: 2019-03-29
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: GE Healthcare, LLC
Product category: device
Product type: Devices

Reported risk: There has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.

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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