Drug recall
Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V1000 and Esprit/V200 Conversion…
FDA recall event 69728 · Class II · Respironics California Inc
Key facts
| Event ID | 69728 |
|---|---|
| Recall numbers | Z-0485-2015 |
| Recalling firm | Respironics California Inc |
| Product type | Devices |
| Products | Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V1000 and Esprit/V200 Conversion Ventilators are microprocessor-controlled, electrically powered mechanical ventilators… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | If the power supply fan mounting screws are installed incorrectly, the ends of the screws may touch the power supply printed circuit board assembly (PCBA) and short to ground. This may prevent the… |
| Initiation date | Oct 29, 2014 |
| Report date | Dec 3, 2014 |
| Termination date | Jun 7, 2016 |
| City | Carlsbad |
| State | CA |
| Country | United States |
| FEI number | 3002470603 |
At a glance
- 1–9 Products in this recall
- 1–9 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: