Device recall
Z-2206-2015: American Science & Engineering Inc,Gemini Cabinet X-ray system.
FDA device recall · Class II · American Science & Engineering, Inc.
Key facts
| Recall number (Z-number) | Z-2206-2015 |
|---|---|
| Recall event | 71696 |
| Product | American Science & Engineering Inc,Gemini Cabinet X-ray system. |
| Product code | RCG |
| Recalling firm | American Science & Engineering, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 22, 2017 |
| FEI number | 1215713 |
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