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

Recall Z-0466-2013 — NeuViz 16 Multi-Sliced CT Scanner System, part number 989605858501. NeuViz Dual series CT Scanner System, part number 989605651321 The NeuViz 16 CT Scanner System can be used as a whole body computed tomography X-ray system featuring a continuously rotating X-ray tube and detector array with mul

U.S. FDA — Device Enforcement · China · 2012-10-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0466-2013
Date of alert: 2012-10-18
Country / jurisdiction: China
Risk level: Class II
Risk type: recall
Brand: Philips And Neusoft Medical Systems Co., Ltd.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 989605858501

Reported risk: The four screws that secure the patient table top to the carrier pulled out and caused the table top to detach. This issue may affect NeuViz Dual and NeuViz 16 scanners.

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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