Cordis recalls SUPER TORQUE MB 5F PIG angiographic catheters (REF 532-598C) due to potential entrapment between devices and vessel walls, risking marker band 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 (REF 532-598C) because improper use may cause the catheter to get stuck between medical devices and blood vessels, potentially leading to marker band movement or dislodgement. This could cause complications during procedures.
The catheter can become trapped between medical devices and blood vessel walls during procedures. This entrapment may cause the marker bands to move or become dislodged, potentially leading to complications.
Healthcare professionals using the catheter for angiographic procedures are most at risk. Patients undergoing these procedures may also be affected if the catheter is used incorrectly.
Check for the model name 'SUPER TORQUE MB 5F PIG' and reference code '532-598C' on the catheter packaging or label. This product was sold by Cordis Corporation.
Verify the model name and reference code on the catheter packaging or label.
The recall is for potential entrapment during improper use, not for normal use. The product is safe when used as intended.
The recall does not specify a remedy, so check with Cordis Corporation for further instructions.
Look for the model name 'SUPER TORQUE MB 5F PIG' and reference code '532-598C' on the packaging or label.
We’ve drafted a message you can send Cordis to request your refund or repair — edit it as you like.
Subject: Recall Z-2432-2021 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-2432-2021 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.
