Device recall
Z-1073-04: TefGen is an implant material which is intended to be used as a temporary…
FDA device recall · Class III · Lifecore Biomedical, Inc.
Key facts
| Recall number (Z-number) | Z-1073-04 |
|---|---|
| Recall event | 29382 |
| Product | TefGen is an implant material which is intended to be used as a temporary space-making barrier over bone or other tissue. |
| Product code | LYC |
| Recalling firm | Lifecore Biomedical, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 22, 2006 |
| 510(k) numbers | K935137 |
| FEI number | 1000115753 |
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