Device recall
Z-0040-2017: Mobile Column TruSystem 7500, Material Number 1717023; Mobile Column TruSystem…
FDA device recall · Class II · Trumpf Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0040-2017 |
|---|---|
| Recall event | 75115 |
| Product | Mobile Column TruSystem 7500, Material Number 1717023; Mobile Column TruSystem 5500, Material Number 1607822 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… |
| 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