Drug recall
Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care…
FDA recall event 66987 · Class II · Smiths Medical ASD, Inc.
Key facts
| Event ID | 66987 |
|---|---|
| Recall numbers | Z-0540-2014 |
| Recalling firm | Smiths Medical ASD, Inc. |
| Product type | Devices |
| Products | Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care areas for the administration of fluids requiring precisely controlled infusion rates. These… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe Infusion Pumps. Smiths Medical has identified an issue with electrical shorting at the AC power receptacle. Shorting can… |
| Initiation date | Nov 22, 2013 |
| Report date | Dec 25, 2013 |
| Termination date | Mar 25, 2015 |
| City | Saint Paul |
| State | MN |
| Country | United States |
| FEI number | 2183502 |
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: