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All product recalls associated with MEDTRONIC ATS MEDICAL, INC..
Total Recalls
2
Past Year
0
Class I (Serious)
0
Most Recent
Oct 2020
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.
There is a potential defect in the seals of the sterile barrier pouch used to package the CryoFlex disposables devices
Medtronic received a complaint from China that the label on the box for an Open Pivot Heart Valve was labeled as Aortic, but the product was Mitral. The valve itself was correctly labeled as Mitral.