Cordis recalls 5F SUPER TORQUE PIG PIGTAIL SPECIAL angiographic catheters (REF SRD7040MB) due to risk of entrapment between devices and vessel walls, potentially causing marker band movement.
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 5F SUPER TORQUE PIG PIGTAIL SPECIAL angiographic catheters (REF SRD7040MB) because improper use may cause the catheter to get stuck between medical devices and blood vessels. This could lead to marker bands moving or becoming dislodged, which might 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 like vessel damage or inaccurate imaging.
Medical professionals using the catheter for angiography procedures are most at risk. Patients undergoing these procedures may also be affected if the catheter is used incorrectly.
Check for the model name '5F SUPER TORQUE PIG PIGTAIL SPECIAL' and reference code SRD7040MB on the catheter packaging or label. This product was sold by Cordis Corporation for medical use.
Identify the model name and reference code on the catheter packaging or label to confirm if it is recalled.
The recall indicates a potential risk of entrapment during use, so it is not recommended for use until the recall remedy is followed.
The recall does not specify a remedy, so check with Cordis Corporation for guidance on next steps.
Look for the model name '5F SUPER TORQUE PIG PIGTAIL SPECIAL' and reference code SRD7040MB on the catheter 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-2429-2021 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-2429-2021 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.
