Device recall
Z-2671-2016: Centricity Laboratory Core Lab System 4.1 The Centricity Laboratory System is…
FDA device recall · Class II · GE Healthcare It
Key facts
| Recall number (Z-number) | Z-2671-2016 |
|---|---|
| Recall event | 64796 |
| Product | Centricity Laboratory Core Lab System 4.1 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 laboratory services and facilities, e.g., the storing and… |
| Product code | JQP |
| Recalling firm | GE Healthcare It |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 29, 2017 |
| 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