Drug recall
The Centricity Laboratory System is intended to be an information system designed to support the clinical and…
FDA recall event 64789 · Class II · GE Healthcare It
Key facts
| Event ID | 64789 |
|---|---|
| Recall numbers | Z-1585-2013 |
| Recalling firm | GE Healthcare It |
| Product type | Devices |
| Products | The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated with the provision and utilization of clinical… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | If environment variables MICRO_CORRECT_MSG_TYPE and CORRECT_MSG_TYPE are set to different values, in Microbiology result entry when released results (Final Report released) are changed and the… |
| Initiation date | Nov 20, 2012 |
| Report date | Jul 3, 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: