Device recall
Z-2563-2011: GE Centricity Laboratory Instrument Interface to Data Innovations Instrument…
FDA device recall · Class II · Ge Healthcare It
Key facts
| Recall number (Z-number) | Z-2563-2011 |
|---|---|
| Recall event | 58676 |
| Product | GE Centricity Laboratory Instrument Interface to Data Innovations Instrument Manager software; GE Healthcare IT Solutions, Barrington, IL 60010. The Centricity Laboratory is designed to facilitate the general clinical, anatomic pathology and cytology laboratory workflow such as order entry, results… |
| Product code | JQP |
| Recalling firm | Ge Healthcare It |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 4, 2011 |
| FEI number | 3004526608 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database