Class IIOngoingZ-1511-2025
Cordis US Corp recalls Cordis
product mix-up; Vascular stent labeled as one size but contains a different size.
Cordis US CorpFLApr 9, 2025
Cordis US Corp recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–3 of 3 recalls
Class IIOngoingZ-1510-2025
Cordis US Corp recalls Cordis
product mix-up; Vascular stent labeled as one size but contains a different size.
Cordis US CorpFLApr 9, 2025
Class IIOngoingZ-1330-2025
Cordis US Corp recalls Vista Brite Tip
Catheter manufactured at the incorrect length.
Cordis US CorpFLMar 19, 2025