FDA Device recall Z-2945-2018
Ceterix Disposable Knot Pusher / Suture Cutter
- FDA Device
- Class II
- terminated
- Published 2018-09-05
On 2018-09-05 the FDA classified a Class II recall of Ceterix Disposable Knot Pusher / Suture Cutter by Ceterix Orthopedics, citing possible nonconforming blades may result in a higher than specified cut force required to cut the suture.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2945-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-16 |
| Published | 2018-09-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ceterix Orthopedics |
| Distribution | n/a |
Product
Ceterix Disposable Knot Pusher / Suture Cutter; NovoCut Suture Manager. Model# CTX-C001. orthopedic arthroscopic accessory.
Reason
Possible nonconforming blades may result in a higher than specified cut force required to cut the suture.
Identifiers
| code_info | Lot#M180018 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2945-2018%22
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