FDAOctober 13, 2015device
NovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic Surgery: Intended for use in arthroscopic surgery.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The NovoCut Suture Manager device may cut the suture during knot tensioning and this may cause the suture knot to unravel.
What to do
FDA enforcement status: Terminated
Brands named
ceterix orthopedicsceterix
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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