Drug recall
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092
FDA recall event 73315 · Class II · CareFusion 303, Inc.
Key facts
| Event ID | 73315 |
|---|---|
| Recall numbers | Z-1239-2016 |
| Recalling firm | CareFusion 303, Inc. |
| Product type | Devices |
| Products | Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | CareFusion is recalling the Alaris PC unit because a component on the PC unit power supply may cause a "System Error" or "Missing Battery" error code (120.4630). |
| Initiation date | Feb 12, 2016 |
| Report date | Mar 30, 2016 |
| Termination date | Jun 23, 2017 |
| 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: