Device recall
Z-1002-03: Drill bits used in ENDOTINE Forehead 3.5 and 3.0, Catalog Number: CFD-010-4203…
FDA device recall · Class II · Coapt Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1002-03 |
|---|---|
| Recall event | 26449 |
| Product | Drill bits used in ENDOTINE Forehead 3.5 and 3.0, Catalog Number: CFD-010-4203 and CFD-010-4303 |
| Product code | --- |
| Recalling firm | Coapt Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 23, 2003 |
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