Device recall
Z-1786-2008: Keramos Replacement Polyethylene Liner, 52mm; Cat. #496-28-052; Sterile, Single…
FDA device recall · Class II · Encore Medical, Lp
Key facts
| Recall number (Z-number) | Z-1786-2008 |
|---|---|
| Recall event | 47870 |
| Product | Keramos Replacement Polyethylene Liner, 52mm; Cat. #496-28-052; Sterile, Single Use; distributed by Encore Medical, L.P., Austin, TX 78758. |
| Product code | MRA |
| Recalling firm | Encore Medical, Lp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 21, 2009 |
| FEI number | 1000116912 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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