FDA recall record

Cordis US Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F recall — FDA Z-1510-2025

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

Class IIclassification
Z-1510-2025official record ID
Apr 9, 2025report date

Recall record at a glance

Official recordZ-1510-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCordis US Corp
Report dateApr 9, 2025
Recall initiation dateMar 4, 2025
Quantity20 units
LocationMiami Lakes, FL, United States

Official product description

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

Why the product was recalled

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

Distribution information

US Distribution to states of: AR, AZ, FL, NJ, TN; and OUS Foreign country of: Japan

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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