Cordis recalls 5F Universal Flush F4 Super Torque MB Angiographic Catheters (REF SRD6785MB) 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 a specific type of angiographic catheter because it can get stuck between medical devices and blood vessels, which might cause the marker bands to move or come loose. This could lead to complications during procedures.
The catheter's marker bands could move or become dislodged if it gets trapped between endovascular devices and the vessel wall during use. This might cause complications during medical procedures.
Healthcare professionals using this catheter for medical procedures are most at risk. Patients receiving these procedures may also be affected if the catheter is used incorrectly.
Check for the model name '5F UNIVERSAL FLUSH F4 SUPER TORQUE MB' and reference number SRD6785MB on the catheter. This product was sold with all codes.
Look for the model name '5F UNIVERSAL FLUSH F4 SUPER TORQUE MB' and reference number SRD6785MB on the catheter.
The recall states the catheter may be used in a way that causes entrapment, but it does not specify that it is dangerous if used correctly.
The recall record does not specify a remedy, so no action is required beyond checking if you have the product.
Check for the model name '5F UNIVERSAL FLUSH F4 SUPER TORQUE MB' and reference number SRD6785MB on the catheter.
We’ve drafted a message you can send Cordis to request your refund or repair — edit it as you like.
Subject: Recall Z-2428-2021 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-2428-2021 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.
