Device recall
Z-1014-04: Trinica Bone Tap Instrument, Catalog Number 07.00168.001, sold separately and as…
FDA device recall · Class II · Zimmer Spine, Inc.
Key facts
| Recall number (Z-number) | Z-1014-04 |
|---|---|
| Recall event | 29200 |
| Product | Trinica Bone Tap Instrument, Catalog Number 07.00168.001, sold separately and as part of Zimmer Spine Trinica Anterior Cervical Plating Instrument sets (catalog numbers 07.00215.001 and 07.00546.001). Only the Trinica Bone Tap Instruments are being recalled from the sets. |
| Product code | HWX |
| Recalling firm | Zimmer Spine, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 3, 2005 |
| 510(k) numbers | K022344 |
| FEI number | 1000115775 |
At a glance
- 1–9 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