PlainRecalls
FDA Devices Moderate Class II Ongoing

Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only

Reported: April 9, 2025 Initiated: March 4, 2025 #Z-1510-2025

Product Description

Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only

Reason for Recall

product mix-up; Vascular stent labeled as one size but contains a different size.

Details

Recalling Firm
Cordis US Corp
Units Affected
20 units
Distribution
US Distribution to states of: AR, AZ, FL, NJ, TN; and OUS Foreign country of: Japan
Location
Miami Lakes, FL

Frequently Asked Questions

What product was recalled?
Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only. Recalled by Cordis US Corp. Units affected: 20 units.
Why was this product recalled?
product mix-up; Vascular stent labeled as one size but contains a different size.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 9, 2025. Severity: Moderate. Recall number: Z-1510-2025.