Device recall
Z-0281-2018: Zimmer Dental Instrument Kit System, Tapered Screw-Vent Implant System surgical…
FDA device recall · Class II · Zimmer Dental Inc
Key facts
| Recall number (Z-number) | Z-0281-2018 |
|---|---|
| Recall event | 78321 |
| Product | Zimmer Dental Instrument Kit System, Tapered Screw-Vent Implant System surgical kit, starter, Ref STRKIT. The label shows the product is Manufactured by Zimmer Dental Inc., Carlsbad, CA. Endosseous dental implant accessories are manually powered devices intended to aid in the placement or removal of… |
| Product code | NDP |
| Recalling firm | Zimmer Dental Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2019 |
| FEI number | 1038806 |
At a glance
- None 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