Device recall
Z-0788-2016: Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material…
FDA device recall · Class II · Biomet France SARL
Key facts
| Recall number (Z-number) | Z-0788-2016 |
|---|---|
| Recall event | 73141 |
| Product | Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures. Endobon Xenograft Granules, Bone Grafting Material, Synthetic are used in the following dental and/or surgical procedures: " Alveolar ridge augmentation/reconstruction, " Sinus… |
| Product code | LYC |
| Recalling firm | Biomet France SARL |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2017 |
| 510(k) numbers | K110449 |
| FEI number | 3006946279 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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