Device recall
Z-0250-2016: NovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic…
FDA device recall · Class II · Ceterix Orthopedics, Inc.
Key facts
| Recall number (Z-number) | Z-0250-2016 |
|---|---|
| Recall event | 72500 |
| Product | NovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic Surgery: Intended for use in arthroscopic surgery. |
| Product code | NBH |
| Recalling firm | Ceterix Orthopedics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 12, 2016 |
| 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