Device recall
Z-1012-2012: Model #03001-02: Periophil Biphasic, Synthetic Biphasic Dental Bone Graft…
FDA device recall · Class II · Cytophil, Inc
Key facts
| Recall number (Z-number) | Z-1012-2012 |
|---|---|
| Recall event | 61044 |
| Product | Model #03001-02: Periophil Biphasic, Synthetic Biphasic Dental Bone Graft Granules, 1.0 cc. Model # 03003-01 Periobase Biphasic: Periobase, Synthetic Biphasic Dental Bone Biphasic Granules, 0.5 cc. Model #03002-01: Periobone Biphasic, Synthetic HA/TCP Dental Bone Graft Biphasic Granules, 0.5 cc… |
| Product code | LYC |
| Recalling firm | Cytophil, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2012 |
| 510(k) numbers | K092788 |
| FEI number | 3007225376 |
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