Device recall
Z-3061-2017: Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat…
FDA device recall · Class II · Shippert Medical Technologies
Key facts
| Recall number (Z-number) | Z-3061-2017 |
|---|---|
| Recall event | 77518 |
| Product | Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat transfer and liposuction. |
| Recalling firm | Shippert Medical Technologies |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 30, 2024 |
| FEI number | 3008719017 |
At a glance
- None 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