Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause delayed treatment or clotting risks.
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An occluded, partially or fully, and/or uncured or excessive MDX may dislodge from the catheter lead to full catheter obstruction resulting in delay to treatment and partial obstruction resulting in reduced flow, or particulate dislodgement that may result in delay to treatment, hemolysis, embolism/embolus or thrombosis/thrombus
Covidien is recalling certain dialysis catheters due to a risk of blockage from excessive silicone lubricant. This could delay treatment or cause blood clots in patients needing dialysis.
The catheter tip can become blocked by silicone lubricant (MDX) that coats it. This blockage may cause treatment delays or blood clots, which can be serious for dialysis patients.
Patients using dialysis treatments with this specific catheter model are most at risk. Healthcare providers who use these catheters for acute dialysis procedures may also be affected.
Check for the model name 'MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, PASS Tray' with lot numbers starting with 2200400292.
If you experience delayed treatment or reduced blood flow, contact your healthcare provider immediately.
Reach out to Covidien for guidance on whether your catheter is affected and next steps.
The recall indicates a potential risk of blockage from silicone lubricant, so it is not recommended for use without checking with the manufacturer.
Contact Covidien to determine if your specific catheter is affected and follow their instructions.
Look for the model name and lot numbers starting with 2200400292 on the catheter packaging.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2377-2023 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2377-2023 from Covidien. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
