RecallDepth

DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a minimally invasive, catheter-based OAS designed for improving luminal diameter in patients with peripheral arterial disease (PAD). PAD is caused by the accumulation of plaque in the arteries of the leg or foot and reduces blood flow that may lead to pain, tissue loss, and eventual foot amputation, leg amputation or death. The system treats a broad range of plaque types in the lower limbs The DIAMONDBACK 360 Peripheral Orbital Atherectomy System is 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. The OAS supports removal of stenotic material from artificial arteriovenous dialysis fistulae (AV shunt). The system is a percutaneous orbital atherectomy system indicated as a therapy in patients with occluded hemodialysis grafts who are acceptable candidates for percutaneous transluminal angioplasty. The Stealth 360 Orbital PAD System is 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.

This recall has been terminated (originally issued February 22, 2017).

Company
Cardiovascular Systems Inc
Recall Initiated
December 7, 2016
Posted
February 22, 2017
Terminated
March 23, 2017
Recall Number
Z-1230-2017
Quantity
8 units
Firm Location
Saint Paul, MN
Official Source
View on FDA website ↗

Reason for Recall

CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.

Distribution

Nationwide Distribution to LA, MS, SC, TX

Lot / Code Info

Lot: 171686, Expiration: 2018-09-30

Root Cause

Employee error

Action Taken

Cardiovascular Systems, Inc. sent an Urgent Medical Device Recall letter, dated 12/07/2016, to all affected customers. The letter identified affected product , stated the reason for recall, asked for product to be returned to CSI. Questions can be directed to Customer Service at 877-274-0901.

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