Cardiovascular Systems recalls some Diamondback devices on embolism risk

Cardiovascular Systems recalls some of its Diamondback 360 orbital atherectomy devices on the risk that a component could fracture during the procedure, possibly causing an embolism.

keys:

Cardiovascular Systems Inc., Food & Drug Administration (FDA)

News Well, Atherectomy, Peripheral Artery Disease, Recalls, Regulatory/Compliance

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