Device recall
Z-2421-2011: Ringloc + Acetabular Shell limited hole finned 46 mm Size 22 porous coat, for…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-2421-2011 |
|---|---|
| Recall event | 58663 |
| Product | Ringloc + Acetabular Shell limited hole finned 46 mm Size 22 porous coat, for uncemented use, sterile, REF 16-104146, Biomet Orthopedics, Warsaw, IN. Intended Use: The Porous Plasma Spray (PPS) Ringloc Acetabular System is intended to replace the natural acetabulurn damaged by disease, trauma or… |
| Product code | KWA |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 16, 2011 |
| 510(k) numbers | K093235 |
| FEI number | 1825034 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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