Medtronic recalls specific DxTerity Diagnostic Catheters due to potential incorrect size labeling on the box, which could lead to improper use. Affected units have a 6F color code on the box but are labeled 5F inside.
The color coded French size indicator on the outer box may incorrectly reflect a 6 French size, rather than the correct 5 French size. The catheters inside the carton are the correct DXT5JL40 item, the inner pouch has correct 5F labeling, information and configuration details.
Medtronic is recalling certain DxTerity Diagnostic Catheters because the outer box incorrectly shows a 6 French size instead of the correct 5 French size. This could lead to using the wrong size catheter, which might cause complications during medical procedures.
The outer box of the catheter has a color code that may incorrectly indicate a 6 French size, while the inner pouch correctly labels it as 5 French. Using the wrong size could lead to improper placement or complications during medical procedures.
Healthcare professionals using the recalled catheters for medical procedures are most at risk. Patients receiving these catheters during procedures may be affected if the wrong size is used.
Check the box for a 6F color code. The catheter is labeled DXT5JL40 with 5F inside the pouch. The UDI is 20643169689309 and lot number 60074805.
Look for a 6F color code on the outer box of the catheter.
The outer box may incorrectly show a 6 French size instead of the correct 5 French size, which could lead to using the wrong size during medical procedures.
Check for a 6F color code on the box. The catheter is labeled DXT5JL40 with 5F inside the pouch and has UDI 20643169689309 and lot number 60074805.
The recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-1479-2018 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-1479-2018 from Medtronic Vascular. 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.
