Device recall
Z-0996-2009: Zimmer Most Hinged Tibia Baseplate Spacer, size 1, 6 mm, sterile, Zimmer…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0996-2009 |
|---|---|
| Recall event | 51039 |
| Product | Zimmer Most Hinged Tibia Baseplate Spacer, size 1, 6 mm, sterile, Zimmer, Warsaw, IN; REF 5020-06-001. Component used to augment uni- and bi-compartmental defects and is manufactured from Ti-6A1-4V Alloy. |
| Product code | KRO |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 12, 2009 |
| 510(k) numbers | K013031 |
| FEI number | 1000220733 |
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