Device recall
Z-1549-2013: Aperio ScanScope System. Aperio ScanScope Models, XT, AT, AT Turbo, CS and CSO…
FDA device recall · Class II · Aperio Technologies Inc
Key facts
| Recall number (Z-number) | Z-1549-2013 |
|---|---|
| Recall event | 33728 |
| Product | Aperio ScanScope System. Aperio ScanScope Models, XT, AT, AT Turbo, CS and CSO. Automated digital slide creation and viewing device. It is intended to create and view electronic image files representative of tissue specimens fixed to glass slides. |
| Product code | IBM |
| Recalling firm | Aperio Technologies Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 25, 2013 |
| FEI number | 3006791373 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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