Drug recall
Newport HT70 and HT70 Plus Ventilators, Model Number: HT70 and HT70 Plus. Product Usage: The HT70 ventilator…
FDA recall event 62856 · Class I · Newport Medical Instruments Inc
Key facts
| Event ID | 62856 |
|---|---|
| Recall numbers | Z-2250-2012 |
| Recalling firm | Newport Medical Instruments Inc |
| Product type | Devices |
| Products | 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… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | May emit a continuous high priority alarm and the ventilator may stop ventilating, due to a component failure on the control board. |
| Initiation date | Aug 3, 2012 |
| Report date | Sep 12, 2012 |
| Termination date | Apr 14, 2014 |
| City | Costa Mesa |
| State | CA |
| Country | United States |
| FEI number | 2023050 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: