Drug recall
Centricity Perinatal and Centricity Intensive Care is intended to be used in clinical departments healthcare…
FDA recall event 64805 · Class II · GE Healthcare It
Key facts
| Event ID | 64805 |
|---|---|
| Recall numbers | Z-0337-2014 |
| Recalling firm | GE Healthcare It |
| Product type | Devices |
| Products | Centricity Perinatal and Centricity Intensive Care is intended to be used in clinical departments healthcare delivery systems such as a Labor and Delivery, Postpartum Maternal Care, newborn Nursery… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 1) Under rare network conditions, a Centricity Perinatal process may maintain an incorrect count of Patient slots in use which may lead to an inability to access the patient roster. The user is… |
| Initiation date | Mar 11, 2013 |
| Report date | Nov 27, 2013 |
| Termination date | Jun 10, 2016 |
| City | Barrington |
| State | IL |
| Country | United States |
| FEI number | 3004526608 |
At a glance
- 1–9 Products in this recall
- 1–9 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: