Cordis recalls specific Smart Control Vascular Stent System models due to size mix-up risk. This could lead to incorrect implantation during procedures.
product mix-up; Vascular stent labeled as one size but contains a different size.
Cordis is recalling a specific vascular stent system model because it was labeled as one size but contains a different size. Using this incorrect size could lead to improper implantation during medical procedures.
The stent system is labeled for one size but contains a different size. This mix-up could result in incorrect implantation during procedures, potentially causing complications.
Medical professionals using the recalled stent system for vascular procedures. Patients receiving the stent during procedures are at risk if the incorrect size is used.
Check for the model name 'Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only' and lot number 18298568/UDI:(01)20705032024430.
Verify the model name and lot number to confirm if your stent system is recalled.
The recall indicates a size mix-up hazard, so it is not safe to use without verifying the correct model.
Check the model name and lot number to see if it is recalled; if recalled, contact Cordis for guidance.
Look for the model name 'Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Only' and lot number 18298568/UDI:(01)20705032024430.
We’ve drafted a message you can send Cordis to request your refund or repair — edit it as you like.
Subject: Recall Z-1511-2025 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-1511-2025 from Cordis. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
