Device recall
Z-0176-2014: Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen the…
FDA device recall · Class II · Pinook-Usa
Key facts
| Recall number (Z-number) | Z-0176-2014 |
|---|---|
| Recall event | 66191 |
| Product | Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen the abdominal muscles. |
| Product code | NGX |
| Recalling firm | Pinook-Usa |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 29, 2016 |
| FEI number | 3008113239 |
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