Device recall
Z-0298-2009: "LOCATOR Abutment for 5.7 Screw-Vent & Compatibles." Zest Anchors, Inc. Product…
FDA device recall · Class III · Zest Anchors Inc
Key facts
| Recall number (Z-number) | Z-0298-2009 |
|---|---|
| Recall event | 48645 |
| Product | "LOCATOR Abutment for 5.7 Screw-Vent & Compatibles." Zest Anchors, Inc. Product is sold for use with any Zimmer Dental 5.7 mm diameter Tapered Screw-Vent Implant. The product is used with supra-gingival, universal hinge, resilient overdenture attachment for endosseous implants. |
| Product code | DZE |
| Recalling firm | Zest Anchors Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 2, 2008 |
| 510(k) numbers | K994257 |
| FEI number | 2023950 |
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