Device recall
Z-0994-04: T2 Proximal Humeral System Targeting Arm. Catalog number 1806-2035.
FDA device recall · Class III · Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-0994-04 |
|---|---|
| Recall event | 28821 |
| Product | T2 Proximal Humeral System Targeting Arm. Catalog number 1806-2035. |
| Product code | LXH |
| Recalling firm | Howmedica Osteonics Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 3, 2004 |
| FEI number | 3003070421 |
At a glance
- None 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