Device recall
Z-0041-2017: Stationary Column TruSystem 7599, Material Number 1717020 Patient positioning…
FDA device recall · Class II · Trumpf Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0041-2017 |
|---|---|
| Recall event | 75115 |
| Product | Stationary Column TruSystem 7599, Material Number 1717020 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Also, patient transport on the operating table top from a patient transfer system to the operating theater of from the… |
| Product code | JEA |
| Recalling firm | Trumpf Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 2, 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