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Recall Observatory FDA recall evidence

Device product

CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000. Product Usage: Usage: The pump is a component of the OAS that provides the pumping mechanism and power to the OAD. The pump does not have an indication independent from that of the systems. The Indications for Use for the peripheral and coronary systems are provided below: Peripheral: The DIAMONDBACK 360¿ and STEALTH Peripheral Orbital Atherectomy Systems are percutaneous orbital atherectomy systems 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 systems are percutaneous orbital atherectomy systems indicated as therapy in patients with occluded hemodialysis grafts who are acceptable candidates for percutaneous transluminal angioplasty. Coronary: The DIAMONDBACK 360 Coronary Orbital Atherectomy System (OAS) is a percutaneous orbital atherectomy system 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

Z-3021-2018

April 13, 2018

Class II

Product summary

Firm
Cardiovascular Systems Inc
Event
Event 80765
Status
Terminated
Classification
Class II
Quantity
18
Official record key
device-enforcement:Z-3021-2018

Official wording

Reason: The pumps may switch to stand-by during use requiring the pump to be reset prior to continuing treatment.

Code information: Lot 126925, 168143, 127026, 146337, 171566, 148400, 182537, 154011, 54512A, 62814B, 124927, 145946, and 127026

Distribution pattern: US Nationwide Distribution in the states of AZ, CA, FL, GA, IL, MO, and TX

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The pumps may switch to stand-by during use requiring the pump to be reset prior to continuing treatment.