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

Recall Z-0979-2015 — Various Brilliance and Ingenuity Computed Tomography X-ray systems; one unit per package Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. This device may include signal analysis and d

U.S. FDA — Device Enforcement · United States · 2014-12-08 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0979-2015
Date of alert: 2014-12-08
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Philips Medical Systems (Cleveland) Inc
Product category: device
Product type: Devices

Reported risk: Improper assembly of the vertical motor/brake system may lead to uncommanded vertical motion.

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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