Cardiovascular Systems Inc: 8 recalls on record

Recalls filed with 1 agency: FDA (8).

First recall on record: July 18, 2012. Most recent: February 14, 2018.

Risk classification: Class I: 2 · Class II: 5 · Class III: 1

Most recent recalls

DateAgencyProduct
February 14, 2018FDAPeripheral Diamondback 1.50 Solid OAD, a percutaneous orbital atherectomy system indicate…Z-0506-2018
May 31, 2017FDACSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-1001…Z-2122-2017
May 3, 2017FDAViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01…Z-1877-2017
March 1, 2017FDADIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Athere…Z-1230-2017
April 1, 2015FDADiamondback 360 Coronary Orbital Atherectomy System, Model Number: DBEC-125. The syste…Z-1290-2015
August 20, 2014FDACSI Cardiovascular Systems, Inc., Diamondback 360 Peripheral Orbital Atherectomy System, …Z-2155-2014
March 5, 2014FDACSI, Diamondback 360 Coronary Orbital Atherectomy System, Part Number 70058-02, Model Num…Z-1095-2014
July 18, 2012FDACSI Stealth 360-degree Orbital Atherectomy Device (OAD), Part Number 70056-11, Model Numb…Z-1959-2012

Questions about this company

How many recalls does Cardiovascular Systems Inc have?
Recalert has 8 U.S. recalls on record for Cardiovascular Systems Inc, published between July 18, 2012 and February 14, 2018.
What was the most recent Cardiovascular Systems Inc recall?
FDA recall Z-0506-2018, published February 14, 2018: 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 acc…
Which agencies have handled Cardiovascular Systems Inc recalls?
Cardiovascular Systems Inc appears as the recalling firm in recalls from: FDA (8).

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