Device recall
Z-1444-2009: Sybaritic, NannoLight MP50. Model Numbers and Description: 1.) 304207-MP 220…
FDA device recall · Class II · Sybaritic, Inc
Key facts
| Recall number (Z-number) | Z-1444-2009 |
|---|---|
| Recall event | 51704 |
| Product | Sybaritic, NannoLight MP50. Model Numbers and Description: 1.) 304207-MP 220 Volt, Multi-Platform configuration (able to attach optional laser handpiece when purchased separately), Subassembly (unit only, no safety glasses, owner's manual, etc. included); 2.) 404207 Completed unit (safety glasses… |
| Product code | GEX |
| Recalling firm | Sybaritic, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 5, 2012 |
| 510(k) numbers | K082033 |
| FEI number | 2131125 |
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