Drug recall
Alaris Pump Module model 8100. Subsequent product code: FPA The Pump module is intended for facilities that…
FDA recall event 55121 · Class I · CareFusion 303, Inc.
Key facts
| Event ID | 55121 |
|---|---|
| Recall numbers | Z-2185-2012 |
| Recalling firm | CareFusion 303, Inc. |
| Product type | Devices |
| Products | Alaris Pump Module model 8100. Subsequent product code: FPA The Pump module is intended for facilities that utilize infusion for the delivery of fluids, medications, blood, and blood products using… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The recall was initiated because Carefusion identified a potential risk associated with the Alaris Pump module model 8100. Carefusion has received reports of customers experiencing motor stalls during… |
| Initiation date | Jun 29, 2012 |
| Report date | Aug 22, 2012 |
| Termination date | Aug 26, 2015 |
| 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: