FDAOctober 31, 2016device

ELCA Coronary Atherectomy Catheter. Models: 110-001, 110-002, 110-004, 114-009, 117-016, 117-205, 120-009 The Laser Catheters are used in conjunction with the Spectranetics CVX-300¿ Excimer Laser System and are intended for use in patients with single or multivessel coronary artery disease, eithe...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Spectranetics Corporation announces a voluntary field action for the Turbo Elite Atherectomy Catheter, ELCA Coronary Atherectomy Catheter, and Bridge Occlusion Balloon due to potentially compromised integrity of the outer sterile packaging.

What to do

FDA enforcement status: Terminated

Brands named

spectranetics

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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