Fremont, CA, United States
Ceterix Orthopedics, Inc. recalls
1 recall recorded since 2018, most recently on 16 May 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 16 May 2018
- Terminated
- 24 August 2020
- Reason
- Possible nonconforming blades may result in a higher than specified cut force required to cut the suture.
- Distribution
- United States distribution.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2945-2018
- Ceterix Disposable Knot Pusher / Suture Cutter; NovoCut Suture Manager. Model# CTX-C001. orthopedic arthroscopic accessory.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.