Device recall
Z-0539-05: MOST Options System Porous and Non-Porous Revision Stem Adapters, manufactured…
FDA device recall · Class II · Zimmer Austin, Inc
Key facts
| Recall number (Z-number) | Z-0539-05 |
|---|---|
| Recall event | 30720 |
| Product | MOST Options System Porous and Non-Porous Revision Stem Adapters, manufactured and distributed by Zimmer Austin, Inc., Austin, Texas 78717 |
| Product code | KRO |
| Recalling firm | Zimmer Austin, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 27, 2007 |
| 510(k) numbers | K013031 |
| FEI number | 2935620 |
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