Device recall
Z-1234-2009: Dentsply, MAILLEFER, CYTCO-K TITANIUM POST SYSTEM, dental implant components…
FDA device recall · Class II · Dentsply Worldwide Headqrt
Key facts
| Recall number (Z-number) | Z-1234-2009 |
|---|---|
| Recall event | 51469 |
| Product | Dentsply, MAILLEFER, CYTCO-K TITANIUM POST SYSTEM, dental implant components, Model numbers (SKU): C106KL0050A20 (12 posts) and C117K00000020 (4 posts), Swiss Made, Manufactured for DENTSPLY Maillefer, Johnson City, TN 37604 |
| Product code | ELR |
| Recalling firm | Dentsply Worldwide Headqrt |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 12, 2010 |
| FEI number | 3004884150 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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