Drug recall
Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit…
FDA recall event 72731 · Class II · Teleflex Medical
Key facts
| Event ID | 72731 |
|---|---|
| Recall numbers | Z-0419-2016 |
| Recalling firm | Teleflex Medical |
| Product type | Devices |
| Products | Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product is being recalled due to complaints that the inspiratory and expiratory tubes are transposed. |
| Initiation date | Apr 17, 2014 |
| Report date | Dec 23, 2015 |
| Termination date | Dec 16, 2015 |
| City | Durham |
| State | NC |
| Country | United States |
| FEI number | 3005747797 |
At a glance
- 1–9 Products in this recall
- 10–99 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: