Device recall
Z-2452-2019: Natrelle 410, Highly Cohesive Anatomically Shaped Silicone-Filled Breast Implant…
FDA device recall · Class I · Allergan PLC
Key facts
| Recall number (Z-number) | Z-2452-2019 |
|---|---|
| Recall event | 83500 |
| Product | Natrelle 410, Highly Cohesive Anatomically Shaped Silicone-Filled Breast Implant Biocell Low Height Low Projection, Sterile, for the following style numbers: Syle LL: LL-410135,LL-410180,LL-410210,LL-410240,LL-410300; Style LM: LM-410140, LM-410190, LM-410220, LM-410250, LM-410320; Style LF… |
| Product code | FTR |
| Recalling firm | Allergan PLC |
| Recall class | Class I |
| Status | Open, Classified |
| PMA numbers | P040046 |
| FEI number | 2011068 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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