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

Recall Z-1714-2014 — Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system that is capable of radiographic and fluoroscopic studies used in an interventional setting.

U.S. FDA — Device Enforcement · United States · 2014-05-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1714-2014
Date of alert: 2014-05-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Toshiba American Medical Systems Inc
Product category: device
Product type: Devices

Reported risk: Although the Flat Panel Detector (FPD) touch sensor is activated during use, the error message is displayed and the audible signal continues sounding during the table movement of longitudinal tilt, the movement of longitudinal tilt does not stop.

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.

Recall Z-1714-2014 — Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system that is capable of radiographic and fluoroscopic studies used in an interventional setting.

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