Overview of recall records associated with Cordis US Corp, including dates, categories and classifications where available.
Classification mix: Class II: 5.
product mix-up; Vascular stent labeled as one size but contains a different size.
product mix-up; Vascular stent labeled as one size but contains a different size.
Catheter manufactured at the incorrect length.
Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as…
Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as…
This page summarizes recall records in which the official source identifies Cordis US Corp 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.
