Cordis recalls SUPER TORQUE MB 5F PIG angiographic catheters with marker bands due to potential entrapment between devices and vessel walls, risking marker band movement or dislodgement.
Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a manner that may allow entrapment of the catheter between endovascular devices and the vessel wall, which can lead to marker band movement or dislodgement.
Cordis is recalling its SUPER TORQUE MB 5:5F PIG angiographic catheters with marker bands. The recall is because improper use might cause the catheter to get stuck between medical devices and blood vessels, which could lead to marker bands moving or becoming dislodged.
The catheter can become trapped between medical devices and blood vessel walls during use. This entrapment might cause marker bands to move or become dislodged, potentially causing complications.
Healthcare professionals using the catheter for medical procedures are most at risk. Patients receiving the catheter during procedures may also be affected.
Check for the Cordis SUPER TORQUE MB 5F PIG angiographic catheter with marker bands. The product code is REF 532-598A.
Identify the product by checking for the REF 532-598A code on the catheter.
The catheter may become trapped between medical devices and blood vessel walls, which could cause marker bands to move or become dislodged.
Check the product code on the catheter to confirm if it's affected. The recall does not require immediate action beyond verification.
The recall record does not mention any remedy or fix for this issue.
We’ve drafted a message you can send Cordis to request your refund or repair — edit it as you like.
Subject: Recall Z-2430-2021 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-2430-2021 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.
