Medtronic Confida Expandable Sheath, REF CES122230 recall — FDA Z-2039-2020
Increased risk of events associated with vascular complications (bleeding, hematoma, and dissection)
Overview of recall records associated with Medtronic Vascular Galway DBA Medtronic Ireland, including dates, categories and classifications where available.
Classification mix: Class I: 1.
Increased risk of events associated with vascular complications (bleeding, hematoma, and dissection)
This page summarizes recall records in which the official source identifies Medtronic Vascular Galway DBA Medtronic Ireland 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.