Drug recall
Newport Medical HT70 and HT70- Plus Ventilators, Rx Only Product Usage: The Newport HT70 family of ventilators…
FDA recall event 76891 · Class I · Newport Medical Instruments Inc
Key facts
| Event ID | 76891 |
|---|---|
| Recall numbers | Z-1874-2017 |
| Recalling firm | Newport Medical Instruments Inc |
| Product type | Devices |
| Products | 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… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Medtronic is issuing a voluntary field corrective action for all its Newport" HT70 and Newport" HT70 Plus ventilators because they may shutdown spontaneously during normal operation without an… |
| Initiation date | Mar 30, 2017 |
| Report date | May 10, 2017 |
| Termination date | Jul 18, 2020 |
| 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: