Device recall
Z-1065-04: Sollux Systeme commercial tanning beds; Soleil Systems, Inc. The following…
FDA device recall · Class II · Soleil Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1065-04 |
|---|---|
| Recall event | 29737 |
| Product | Sollux Systeme commercial tanning beds; Soleil Systems, Inc. The following models are affected by this recall: a) Sollux Systeme 32 - 32 x 100 w tanning bulbs, no facial tanner bulbs b) Sollux Systeme 32.3 - 32 x 100 w tanning bulbs, plus 3 x 400 w facial tanner bulbs c) Sollux Systeme 36 - 18 x 100… |
| Product code | U--19 |
| Recalling firm | Soleil Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 28, 2006 |
| FEI number | 3004002126 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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