FDAMarch 4, 2015device

Diamondback 360 Coronary Orbital Atherectomy System, Model Number: DBEC-125. The system is indicated to facilitate stent delivery in patients with coronary artery disease (CAD) who are acceptable candidates for PTCA or stenting due to de novo, severely calcified coronary artery lesions.

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

The hazard

The OAD saline sheath outer layer may flake off from the catheter due to friction between the outer material layer and corresponding materials it may come in contact with during clinical use. If the material is large enough, it has the potential to cause a flow limiting embolism.

What to do

FDA enforcement status: Terminated

Brands named

cardiovascular systemscardiovascular

Recall history

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

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