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All product recalls associated with Medtronic Inc. Cardiac Rhythm Managment.
Total Recalls
1000
Past Year
583
Class I (Serious)
91
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
Incorrect micro-organism-- .Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).
The recalled gas regulators were manufactured from March 2007 through May 2007 and installed on natural gas or LP-gas supply systems in homes and small commercial buildings. The recalls involves model HSR natural gas regulators and LP-gas regulators with model numbers 67CD, 67CH, 67CN, and 67CW, HSRL, R622, R622E, R622H, R632, R642, R652, R652E, R122H, R222, or R232. The model number can be found on a white label attached to the regulator spring case. The date of manufacture is also stamped on the regulator.