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

Recall Z-0973-2017 — OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac,

U.S. FDA — Device Enforcement · United States · 2016-12-19 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0973-2017
Date of alert: 2016-12-19
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: GE OEC Medical Systems, Inc
Product category: device
Product type: Devices

Reported risk: GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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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