Loading...
Loading...
All product recalls associated with Medtronic CardioVascular.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
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.
Sterility compromised: Device sterility may be compromised as evidenced by a loss of outer package integrity.
The recalled home gyms are equipped with pulleys, resistance rods, and other equipment, which allow the user to perform a variety of exercises. "Bowflex Ultimate 2" is written on the vertical part of the frame.
Inaccurate results: A software bug may cause inaccurate wall motion abnormality scoring results to be displayed.