Device recall
Z-2740-2015: DermaPen Pro Model, Micro Needling System, a motorized AC powered surgical…
FDA device recall · Class II · Derma Pen, LLC
Key facts
| Recall number (Z-number) | Z-2740-2015 |
|---|---|
| Recall event | 71149 |
| Product | DermaPen Pro Model, Micro Needling System, a motorized AC powered surgical instrument for dermabrasive use. Each motorized handpiece is packaged within a small box. Each disposable needle cartridge is packaged individually and then placed into boxes of 30 quantities per box. |
| Product code | PIU |
| Recalling firm | Derma Pen, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 31, 2017 |
| FEI number | 3009081613 |
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