Device recall
Z-1129-2012: DirectFRAP (Direct Flourescence Recovery After Photobleaching) Imaging System is…
FDA device recall · Class II · Zeiss, Carl Inc
Key facts
| Recall number (Z-number) | Z-1129-2012 |
|---|---|
| Recall event | 59285 |
| Product | DirectFRAP (Direct Flourescence Recovery After Photobleaching) Imaging System is an extension unit for Axio Observer that is used for microscopic analyses of dynamic processes within living cells. The DirectFRAP module is a component used in conjunction with Laser Scanning Microscopes, Non-Medical… |
| Product code | REK |
| Recalling firm | Zeiss, Carl Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 11, 2012 |
| FEI number | 2431026 |
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