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

Recall Z-2250-2012 — Newport HT70 and HT70 Plus Ventilators, Model Number: HT70 and HT70 Plus. Product Usage: The HT70 ventilator system is intended to provide continuous or intermittent positive pressure mechanical ventilatory support for the care of individuals who require mechanical ventilation through invasive

U.S. FDA — Device Enforcement · United States · 2012-08-03 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2250-2012
Date of alert: 2012-08-03
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Newport Medical Instruments Inc
Product category: device
Product type: Devices

Reported risk: May emit a continuous high priority alarm and the ventilator may stop ventilating, due to a component failure on the control board.

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.

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