# FDA recall Z-2945-2018

> **Ceterix Orthopedics, Inc.** · Class II · device recall initiated 2018-05-16.

## Product

Ceterix Disposable Knot Pusher / Suture Cutter; NovoCut Suture Manager. Model# CTX-C001.  orthopedic arthroscopic accessory.

## Reason for recall

Possible nonconforming blades may result in a higher than specified cut force required to cut the suture.

## Distribution

United States distribution.

## Key facts

- **Recall number:** Z-2945-2018
- **Recalling firm:** Ceterix Orthopedics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-16
- **Report date:** 2018-09-05
- **Termination date:** 2020-08-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fremont, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2945-2018

## Citation

> AI Analytics. FDA recall Z-2945-2018. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2945-2018. Source: US FDA. Licensed CC0.

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