Drug recall
GemStar Pump - Battery Product Usage: The GemStar Pump is a small and lightweight, single channel infusion…
FDA recall event 64839 · Class I · Hospira Inc.
Key facts
| Event ID | 64839 |
|---|---|
| Recall numbers | Z-1159-2013, Z-1160-2013 |
| Recalling firm | Hospira Inc. |
| Product type | Devices |
| Products | GemStar Pump - Battery Product Usage: The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Battery level lower then 2.4 volts results in corrupt history log and loss of data for preview therapy's parameters and causes an 11/004 error resulting in the pump not being able to be used. |
| Initiation date | Mar 18, 2013 |
| Report date | May 8, 2013 |
| Termination date | Mar 7, 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: