Drug recall
Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
FDA recall event 80490 · Class II · Smiths Medical ASD Inc.
Key facts
| Event ID | 80490 |
|---|---|
| Recall numbers | Z-2662-2018 |
| Recalling firm | Smiths Medical ASD Inc. |
| Product type | Devices |
| Products | Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Certain Barrel Clamp Guides may contain a ridge that could potentially lead to spring slippage, resulting in the inability of the pump to recognize a loaded syringe or the pump, misidentifying the… |
| Initiation date | Apr 13, 2018 |
| Report date | Aug 15, 2018 |
| Termination date | Jan 30, 2023 |
| City | Minneapolis |
| State | MN |
| Country | United States |
| FEI number | 3012307300 |
At a glance
- 1–9 Products in this recall
- 1–9 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: