Overview of recall records associated with Medtronic Vascular, including dates, categories and classifications where available.
Classification mix: Class I: 4.
The component part numbers intended for shipment to a third-party, where they are further processed into kits and sterilized were instead shipped directly to customers.
Subsequent failure of catheters in the field and failed quality testing
Subsequent failure of catheters in the field and failed quality testing
Subsequent failure of catheters in the field and failed quality testing
This page summarizes recall records in which the official source identifies Medtronic Vascular as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
