FDASeptember 14, 2017device

Peripheral Diamondback 1.50 Solid OAD, a percutaneous orbital atherectomy system indicated for use as therapy in patients with occlusive atherosclerotic disease in peripheral arteries and who are acceptable candidates for percutaneous transluminal atherectomy.

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

The hazard

Cardiovascular Systems, Inc. (CSI) is removing the products because it was identified that the labeling for two lots of product s were potentially inadvertently switched during production.

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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