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All product recalls associated with Medtronic Cardiovascular Surgery-the Heart Valve Division.
Total Recalls
11
Past Year
0
Class I (Serious)
0
Most Recent
Aug 2014
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 has decided to discontinue production and distribution of this low-volume product.
Mislabeling-- The incorrect Instructions for use may have been included with this product.
Mislabeling-- A lot of 5 mm x 120 mm stents were labeled as 6 mm x 80 mm stents and vice versa.