Device recall
Z-1622-2010: Endotec Prosthesis Shoulder, Titanium Alloy, Sterilized Modular Femoral Stem BP…
FDA device recall · Class II · Endotec, Inc.
Key facts
| Recall number (Z-number) | Z-1622-2010 |
|---|---|
| Recall event | 52527 |
| Product | Endotec Prosthesis Shoulder, Titanium Alloy, Sterilized Modular Femoral Stem BP Shoulder Component: 12mm Modular Femoral Stem, Catalog: 02-21-0103, Lot 02-21-0103ANN374. |
| Product code | JWH |
| Recalling firm | Endotec, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2013 |
| 510(k) numbers | K904880 |
| FEI number | 3004553437 |
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