Medtronic Inc. Cardiac Rhythm Disease Management recalls

Medtronic Inc. Cardiac Rhythm Disease Management has 22 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 14 Oct 2015. The most frequent reason is sterility.

Total recalls22since 2013
Last 12 months0reported
Class I15% of total
Ongoing0latest 14 Oct 2015

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 5%Class II 21 95%Class III 0 0%

Why medtronic inc. cardiac rhythm disease management is recalled

By year

All medtronic inc. cardiac rhythm disease management recalls, newest first

22 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIMedtronic Medical Device Identification Card recalledMedtronic Inc. Cardiac Rhythm Disease ManagementOtherNationwide
DeviceCLASS IIMedtronic CryoConsole recalled by Medtronic Inc. Cardiac RhythmMedtronic Inc. Cardiac Rhythm Disease ManagementOtherNationwide
DeviceCLASS IICovidien Trellis 6 and Trellis 8 Peripheral Infusion recalledMedtronic Inc. Cardiac Rhythm Disease ManagementSterilityNationwide
DeviceCLASS IIMedtronic Dual Chamber Temporary External Pacemaker recalledMedtronic Inc. Cardiac Rhythm Disease ManagementLead & Heavy MetalsNationwide
DeviceCLASS IMedtronic FlexCath Select Steerable Sheath recalledMedtronic Inc. Cardiac Rhythm Disease ManagementOtherNationwide
DeviceCLASS IIMedtronic Select CAP Arterial Cannulae recalledMedtronic Inc. Cardiac Rhythm Disease ManagementForeign MaterialNationwide
DeviceCLASS IIMedtronic Select 3D Arterial Cannulae recalledMedtronic Inc. Cardiac Rhythm Disease ManagementForeign MaterialNationwide
DeviceCLASS IIMedtronic Intersept Custom Tubing Pack which contain Select recalledMedtronic Inc. Cardiac Rhythm Disease ManagementSterilityNationwide
DeviceCLASS IIMedtronic Select 3D Arterial Cannulae recalledMedtronic Inc. Cardiac Rhythm Disease ManagementForeign MaterialNationwide
DeviceCLASS IIMedtronic Select 3D Arterial Cannulae recalledMedtronic Inc. Cardiac Rhythm Disease ManagementSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.