Device recall
Z-2884-2011: LPCCC2: Low Profile Abutment Non-Hexed Castable Cylinder by Biomet 3i Castable…
FDA device recall · Class III · Biomet 3i, LLC
Key facts
| Recall number (Z-number) | Z-2884-2011 |
|---|---|
| Recall event | 58921 |
| Product | LPCCC2: Low Profile Abutment Non-Hexed Castable Cylinder by Biomet 3i Castable cylinders are intended to be used to produce a definitive casting for dental restoration onto which porcelain can then be cast |
| Product code | NHA |
| Recalling firm | Biomet 3i, LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 27, 2011 |
| 510(k) numbers | K092341 |
| FEI number | 1038806 |
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