Drug recall
Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.
FDA recall event 67326 · Class II · CareFusion 303, Inc.
Key facts
| Event ID | 67326 |
|---|---|
| Recall numbers | Z-0931-2014 |
| Recalling firm | CareFusion 303, Inc. |
| Product type | Devices |
| Products | Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a defect in the trifurcated component that could result in a component leak. |
| Initiation date | Jan 16, 2014 |
| Report date | Feb 12, 2014 |
| Termination date | Aug 6, 2014 |
| City | San Diego |
| State | CA |
| Country | United States |
| FEI number | 2016493 |
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: