Drug recall
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…
FDA recall event 67761 · Class II · Hospira Inc.
Key facts
| Event ID | 67761 |
|---|---|
| Recall numbers | V-138-2014 |
| Recalling firm | Hospira Inc. |
| Product type | Veterinary |
| 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 II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Certain Plum A+ fluid shield diaphragms may be out of specification and may cause N250 "Door Open while pumping" or N100 "Unrecognizable Cassette" alarms. Both the N250 and N100 alarm conditions… |
| Initiation date | Mar 12, 2013 |
| Report date | Jul 23, 2014 |
| Termination date | Nov 28, 2016 |
| 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: