Cordis recalls Vista Brite Tip catheters with incorrect length. This may cause improper use during medical procedures. Affected units have specific UDI and lot numbers.
Catheter manufactured at the incorrect length.
Cordis is recalling certain Vista Brite Tip guiding catheters due to being manufactured at the incorrect length. This could lead to improper use during medical procedures if the catheter is too short or too long.
The catheter is manufactured at the incorrect length, which could cause it to be too short or too long for proper use during medical procedures. This might lead to improper placement or complications during interventions.
Healthcare professionals using the catheters for medical procedures are most likely affected. Patients receiving these procedures may be at risk if the catheter length is incorrect.
Check for the UDI: 20705032042991 and lot number 18368326 on the catheter packaging. The product names include Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F.
Look for the UDI: 20705032042991 and lot number 18368326 on the catheter packaging.
Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F.
Check for the UDI: 20705032042991 and lot number 18368326 on the catheter packaging.
The recall record does not specify a remedy, so contact Cordis for further instructions.
We’ve drafted a message you can send Cordis to request your refund or repair — edit it as you like.
Subject: Recall Z-1330-2025 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-1330-2025 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.