Drug recall
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…
FDA recall event 69336 · Class I · Hospira Inc.
Key facts
| Event ID | 69336 |
|---|---|
| Recall numbers | Z-1071-2015, Z-1072-2015, Z-1073-2015, Z-1074-2015, Z-1075-2015 |
| Recalling firm | Hospira Inc. |
| Product type | Devices |
| Products | The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environments. It is a cassette based multi-function infusion system. The Plum A+ allows… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels. |
| Initiation date | Jul 2, 2014 |
| Report date | Mar 4, 2015 |
| Termination date | May 24, 2017 |
| 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: