Home / Recalls / Medical Devices
Ceterix Orthopedics, Inc. recalls NovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic Surgery: Intended for use in arthroscopic
Recalled November 18, 2015 · FDA recall Z-0250-2016 · Ceterix Orthopedics
Hazard
The NovoCut Suture Manager device may cut the suture during knot tensioning and this may cause the suture knot to unravel. · FDA Class II
Units
1364 units
Sold at
Nationwide Distribution
Description
The NovoCut Suture Manager device may cut the suture during knot tensioning and this may cause the suture knot to unravel.
Product
NovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic Surgery: Intended for use in arthroscopic surgery.
Manufacturer(s)
Ceterix Orthopedics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →