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All product recalls associated with Medtronic Inc. Cardiac Rhythm Managment.
Total Recalls
624
Past Year
58
Class I (Serious)
52
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Medtronic Cardiac Rhythm Disease Management has voluntarily suspended worldwide distribution of the Sprint Fidelis family of defibrillation leads because of the potential for lead fractures. In addition, the company recommends against new implants of the leads (Sprint Fidelis Models: 6930, 6931, 6948, 6949). Medtronic, its Independent Physician Quality Panel, and Bruce Lindsay, M.D., Professor of
An issue with the Paceart System - 2006 First Edition (Get Connected Edition) exists. Under certain circumstances, Paceart System Generic ICD reports may not accurately reflect patient VT/VF, SVT/NST and Mode Switch/AT/AF episode detection data. When episode detection data is imported into the Paceart System from certain sources, the Paceart System Generic ICD reports display a zero, suggesting
This recall involves 190 Radial Brake Master Cylinders used on off-road motorcycles. The brake cylinders have an "A" or "B" code on the underside of the lever's pivot bolt. The Magura logo is printed on the cylinder. Brake cylinders without the "A" or "B" markings are not included in this recall.