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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