Drug recall
CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood and blood products through a…
FDA recall event 64204 · Class II · Carefusion 303 Inc
Key facts
| Event ID | 64204 |
|---|---|
| Recall numbers | Z-0832-2013 |
| Recalling firm | Carefusion 303 Inc |
| Product type | Devices |
| Products | CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood and blood products through a needle or catheter inserted into the patient's artery or vein. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | CareFusion is recalling the SmartSite¿ Gravity Blood Set as a result of a potential for separation at the connection of the drip chamber and tubing . The separation may be observed at priming or… |
| Initiation date | Dec 20, 2012 |
| Report date | Feb 27, 2013 |
| Termination date | Jul 25, 2013 |
| City | San Diego |
| State | CA |
| Country | United States |
| FEI number | 3009051210 |
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: