Device recall
Z-0391-2017: OR Table, Top U26 H V, Model # 1909793; OR Table Top U26 H V U, Model # 1909794…
FDA device recall · Class II · Trumpf Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0391-2017 |
|---|---|
| Recall event | 75412 |
| Product | OR Table, Top U26 H V, Model # 1909793; OR Table Top U26 H V U, Model # 1909794; OR Table Top U24 H V, Model # 1909796; OR Table Top U24 H V U, Model # 1909797; OR Table Top U24 H V W, Model # 1909798; OR Table Top U14 H V, Model # 1909799 Product Usage: Patient positioning during surgery, ranging… |
| Product code | JEA |
| Recalling firm | Trumpf Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 6, 2017 |
| FEI number | 3003184737 |
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