Device recall
Z-0040-05: ATO Drill Guide Kit (All Through One Drill Guides Set), model number…
FDA device recall · Class II · Zimmer Spine, Inc.
Key facts
| Recall number (Z-number) | Z-0040-05 |
|---|---|
| Recall event | 29908 |
| Product | ATO Drill Guide Kit (All Through One Drill Guides Set), model number 07.00860.001, product is packaged in trays. |
| Product code | KWQ |
| Recalling firm | Zimmer Spine, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 3, 2005 |
| FEI number | 1000115775 |
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