Device recall
Z-0414-2010: STERIS Harmony LL 500/700 Surgical Light, Vertical Spring-Loaded Arm. Intended…
FDA device recall · Class II · Steris Corp
Key facts
| Recall number (Z-number) | Z-0414-2010 |
|---|---|
| Recall event | 53475 |
| Product | STERIS Harmony LL 500/700 Surgical Light, Vertical Spring-Loaded Arm. Intended for local illumination of the operating and examination area of the patient in treatment rooms. |
| Product code | FTD |
| Recalling firm | Steris Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 1, 2012 |
| 510(k) numbers | K010724 |
| FEI number | 1527821 |
At a glance
- 1–9 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