Drug recall
The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and…
FDA recall event 64263 · Class II · Hospira Inc.
Key facts
| Event ID | 64263 |
|---|---|
| Recall numbers | Z-0283-2014, Z-0284-2014, Z-0285-2014, Z-0286-2014, Z-0287-2014, Z-0288-2014, Z-0289-2014, Z-0290-2014 |
| Recalling firm | Hospira Inc. |
| Product type | Devices |
| Products | The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+3…, The Plum A+ Hyperbaric Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The…, The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Plum A+ infusers have the potential for the distal (occlusion) press sensor pin to break. The distal pressure sensor pin is a part of the overall subsystem that measures the pressure within the distal… |
| Initiation date | Feb 1, 2013 |
| Report date | Nov 20, 2013 |
| Termination date | Dec 6, 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: