Device recall
Z-2406-2011: Newport HT70 Ventilator. Model #HT70, The Newport HT70 ventilator is intended to…
FDA device recall · Class II · Newport Medical Instruments Inc
Key facts
| Recall number (Z-number) | Z-2406-2011 |
|---|---|
| Recall event | 58619 |
| Product | Newport HT70 Ventilator. Model #HT70, The Newport HT70 ventilator is intended to provide continuous or intermittent positive pressure mechanical ventilatory support for the care of individuals who require mechanical ventilation through invasive or noninvasive interfaces. Specifically, the Newport… |
| Product code | CBK |
| Recalling firm | Newport Medical Instruments Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 3, 2011 |
| 510(k) numbers | K090888 |
| FEI number | 2023050 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database