Drug recall
Alaris PCA Pump, Model 8120. The firm name on the label is CareFusion. The Alaris Syringe Pump module and…
FDA recall event 78588 · Class II · CareFusion 303, Inc.
Key facts
| Event ID | 78588 |
|---|---|
| Recall numbers | Z-0322-2018, Z-0323-2018 |
| Recalling firm | CareFusion 303, Inc. |
| Product type | Devices |
| Products | Alaris PCA Pump, Model 8120. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA module are infusion pump modules for the Alaris System. The syringe pump and PCA…, Alaris Syringe Pump, Model 8110. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA module are infusion pump modules for the Alaris System. The syringe pump and… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The syringe plunger grippers may fail to automatically close around the syringe plunger press when the gripper control knob has been closed. |
| Initiation date | Nov 17, 2017 |
| Report date | Jan 17, 2018 |
| Termination date | May 4, 2020 |
| 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: