Cordis recalls SUPER TORQUE MB 5F PIG angiographic catheters (REF 532-598B) due to risk of entrapment between devices and vessel walls, potentially causing 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.
Cord: The Cordis SUPER TORQUE MB 5F PIG angiographic catheter (REF 532-598B) is being recalled because it may get stuck between medical devices and blood vessels, which could cause the marker bands to move or become dislodged. This poses a risk to patients during procedures.
The catheter can become trapped between endovascular devices and blood vessel walls during procedures. This entrapment may cause the marker bands to move or dislodge, potentially leading to complications during medical treatments.
Healthcare professionals using the catheter during medical procedures are most at risk. Patients undergoing angiography may also be affected if the catheter becomes dislodged.
Check for the model name 'SUPER TORQUE MB 5F PIG' and reference number '532-598B' on the catheter. This product was sold by Cordis Corporation.
Verify the model name and reference number on the catheter to confirm it matches the recalled item.
The recall indicates a potential risk of entrapment during procedures, so it is not recommended for use until the recall is addressed.
Look for the model name 'SUPER TORQUE MB 5F PIG' and reference number '532-598B' on the catheter.
The recall does not specify a remedy, so contact Cordis Corporation directly for guidance.
We’ve drafted a message you can send Cordis to request your refund or repair — edit it as you like.
Subject: Recall Z-2431-2021 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-2431-2021 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.
