Device recall
Z-0401-2013: BioPlant, a dental bone grafting material. BioPlant has been assigned the…
FDA device recall · Class II · Kerr Corporation
Key facts
| Recall number (Z-number) | Z-0401-2013 |
|---|---|
| Recall event | 63557 |
| Product | BioPlant, a dental bone grafting material. BioPlant has been assigned the product code LYC (Bone Grafting Material, Synthetic) by the FDA and is classified as a Class II Medical Device. BioPlant is a Class II Medical Device. The Device Listing Number is 0007254. BioPlant is a synthetic, multipurpose… |
| Product code | LYC |
| Recalling firm | Kerr Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 23, 2013 |
| FEI number | 2024312 |
At a glance
- None 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