Drug recall
CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with…
FDA recall event 68955 · Class II · Carefusion 2200 Inc
Key facts
| Event ID | 68955 |
|---|---|
| Recall numbers | Z-2689-2014 |
| Recalling firm | Carefusion 2200 Inc |
| Product type | Devices |
| Products | CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with a ventilator when mechanical ventilation is administered to a patient. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due to a regulatory compliance risk involving a material change. The changes to the gas pathway may potentially impact the… |
| Initiation date | Jul 31, 2014 |
| Report date | Oct 1, 2014 |
| Termination date | Feb 8, 2016 |
| City | Vernon Hills |
| State | IL |
| Country | United States |
| FEI number | 3008002452 |
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: