Device recall
Z-2945-2018: Ceterix Disposable Knot Pusher / Suture Cutter; NovoCut Suture Manager. Model#…
FDA device recall · Class II · Ceterix Orthopedics, Inc.
Key facts
| Recall number (Z-number) | Z-2945-2018 |
|---|---|
| Recall event | 80688 |
| Product | Ceterix Disposable Knot Pusher / Suture Cutter; NovoCut Suture Manager. Model# CTX-C001. orthopedic arthroscopic accessory. |
| Product code | NBH |
| Recalling firm | Ceterix Orthopedics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 2020 |
| FEI number | 3009131204 |
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