Drug recall
Plum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of delivering fluids for a…
FDA recall event 76253 · Class II · Hospira Inc., A Pfizer Company
Key facts
| Event ID | 76253 |
|---|---|
| Recall numbers | Z-1682-2017 |
| Recalling firm | Hospira Inc., A Pfizer Company |
| Product type | Devices |
| Products | Plum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of delivering fluids for a variety of therapies such as parenteral, enteral, or epidural infusions |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Depleted Battery alarm shows instead of Replace Battery. On battery power, ongoing therapy stops, alarms show and sound, pump shuts down after 3 minutes. On AC power, the pump reboots (takes about 25… |
| Initiation date | Dec 30, 2016 |
| Report date | Apr 5, 2017 |
| Termination date | Jul 9, 2019 |
| City | Lake Forest |
| State | IL |
| Country | United States |
| FEI number | 3005579246 |
At a glance
- 1–9 Products in this recall
- None 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: