Device recall
Z-0563-2016: Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted…
FDA device recall · Class II · Trumpf Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0563-2016 |
|---|---|
| Recall event | 72542 |
| Product | Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5 |
| Product code | FSY |
| Recalling firm | Trumpf Medical Systems, Inc. |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K061317, K102758 |
| FEI number | 3003184737 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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