Overview of recall records associated with Cordis Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 18, Class I: 7, Class III: 1.
Due to a labeling error related to the conversion of the inner diameter of the catheter from inches to millimeters. The English dimension is correct and is the primary dimension.
Correction to provide clarification and additional labeling to minimize likelihood on implanting filter backwards.
This page summarizes recall records in which the official source identifies Cordis Corporation 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.
