Device recall
Z-1123-2015: Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1123-2015 |
|---|---|
| Recall event | 70438 |
| Product | Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component. |
| Product code | KWA |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2015 |
| 510(k) numbers | K093235 |
| FEI number | 1825034 |
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