Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

NovoCut Suture Manager Recalled by Ceterix Orthopedics, Inc. Due to The NovoCut Suture Manager device may cut the...

Date: October 13, 2015
Company: Ceterix Orthopedics, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Ceterix Orthopedics, Inc. directly.

Affected Products

NovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic Surgery: Intended for use in arthroscopic surgery.

Quantity: 1364 units

Why Was This Recalled?

The NovoCut Suture Manager device may cut the suture during knot tensioning and this may cause the suture knot to unravel.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Ceterix Orthopedics, Inc.

Ceterix Orthopedics, Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report