Device recall
Z-1874-2017: Newport Medical HT70 and HT70- Plus Ventilators, Rx Only Product Usage: The…
FDA device recall · Class I · Newport Medical Instruments Inc
Key facts
| Recall number (Z-number) | Z-1874-2017 |
|---|---|
| Recall event | 76891 |
| Product | Newport Medical HT70 and HT70- Plus Ventilators, Rx Only Product Usage: The Newport HT70 family of ventilators is intended to provide continuous or intermittent positive pressure mechanical ventilatory support for the care of individuals who require mechanical ventilation through invasive or… |
| Product code | CBK |
| Recalling firm | Newport Medical Instruments Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 18, 2020 |
| 510(k) numbers | K090888, K111146 |
| 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