Device recall
Z-0993-2015: TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR…
FDA device recall · Class II · Maquet Medical Systems USA
Key facts
| Recall number (Z-number) | Z-0993-2015 |
|---|---|
| Recall event | 69560 |
| Product | TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR Integration System is designed to be used as the central operating unit in an operating room. The integration system has two main functions: Recording and distribution of images and videos and interaction with medical and… |
| Product code | OUG |
| Recalling firm | Maquet Medical Systems USA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 17, 2015 |
| FEI number | 3008355164 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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