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Medtronic Cardiovascular Surgery-the Heart Valve Division Recalls
4 recalls on record · February 12, 2014 to August 24, 2016 · Medical Devices
Recalls by year
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16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 24, 2016Medical DevicesFDA
Medtronic Cardiovascular Surgery-the Heart Valve Division recalls Medtronic EnVeo R Delivery Catheter System (DCS), Models: ENVEOR-L, ENVEOR-L-C, and ENVEOR-US. Designed to replace th
Hazard: Potential for vascular trauma with the use of the Medtronic EnVeo R Delivery Catheter System (DCS).
August 12, 2015Medical DevicesFDA
Medtronic Cardiovascular Surgery-the Heart Valve Division recalls EnVeo R Loading System, Model No. LS-EnVeoR-23, LS-EnVeoR-2629, LS-EnVeoR-23-C, LS-EnVeoR-2629-C. Cardiovascular v
Hazard: Medtronic is recalling the EnVeo R Loading Systems because of the presence of particulate.
September 17, 2014Medical DevicesFDA
Medtronic Cardiovascular Surgery-the Heart Valve Division recalls Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012. Used use in conjunction with Hanc
Hazard: Medtronic has decided to discontinue production and distribution of this low-volume product.
February 12, 2014Medical DevicesFDA
Medtronic Cardiovascular Surgery-the Heart Valve Division recalls Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators are used with the Mosaic Porcine Aorti
Hazard: Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator Model 7305 used with the Mosaic Porcine Aortic Bioprosthesis, Model Number 305, because of higher-than-expected transvalvular gradients occurring post implant.