Drug recall
CareFusion Gravity Set, Model #44000-07 The CareFusion Gravity Sets are used to administer fluid and…
FDA recall event 66152 · Class II · CareFusion 303, Inc.
Key facts
| Event ID | 66152 |
|---|---|
| Recall numbers | Z-2281-2013 |
| Recalling firm | CareFusion 303, Inc. |
| Product type | Devices |
| Products | CareFusion Gravity Set, Model #44000-07 The CareFusion Gravity Sets are used to administer fluid and medication through a needle or catheter inserted into the patient's artery or vein. The CareFusion… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | CareFusion is recalling the Gravity Set (Model 44000-07) because of an incorrect expiration date. The affected lot numbers of the Gravity Set are labeled with a 5 year expiration instead of three (3)… |
| Initiation date | Aug 30, 2013 |
| Report date | Oct 2, 2013 |
| Termination date | Dec 26, 2013 |
| 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: