Device recall
Z-0801-2007: Biohorizons 3.0mm Overdenture Implant System, REF 30120S2, (3 mm x12 mm-2mm…
FDA device recall · Class III · BioHorizons Implant Systems Inc
Key facts
| Recall number (Z-number) | Z-0801-2007 |
|---|---|
| Recall event | 37893 |
| Product | Biohorizons 3.0mm Overdenture Implant System, REF 30120S2, (3 mm x12 mm-2mm collar), Biohorizons Implant Systems, Inc., Birmingham, AL 35243 |
| Product code | DZE |
| Recalling firm | BioHorizons Implant Systems Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 11, 2007 |
| 510(k) numbers | K041938 |
| FEI number | 1000592496 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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