Device recall
Z-0799-06: Porous titanium flared rim acetabular shell with three clustered holes in even…
FDA device recall · Class III · Encore Medical, Lp
Key facts
| Recall number (Z-number) | Z-0799-06 |
|---|---|
| Recall event | 34416 |
| Product | Porous titanium flared rim acetabular shell with three clustered holes in even sizes from 48 to 66mm, a hip prosthesis component. The lot number on the product labeling is the unique identifier of this component. |
| Product code | LPH |
| Recalling firm | Encore Medical, Lp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 11, 2006 |
| 510(k) numbers | K950542 |
| FEI number | 1000116912 |
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