Angiodynamics recalls DURAMAX Stacked Tip 28cm kits for possible metal shavings that could cause embolism requiring surgery.
Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
Angiodynamics is recalling DURAMAX Stacked Tip 28cm kits because they may contain metal shavings that could travel to the bloodstream and require surgical removal. This is a serious risk for patients needing long-term vascular access for hemodialysis or apheresis.
The Tri-Ball Tunneler component may have loose metal shavings that can enter the bloodstream. If these shavings travel to critical areas, they could cause blockages requiring surgery to remove.
Patients using this kit for hemodialysis or apheresis are most at risk. Anyone with the product number H787103028041 or lot number 5805840 should check if they own it.
Check for product number H787103028041 or lot number 5805840 on the kit. This kit is intended for long-term vascular access in hemodialysis and apheresis treatments.
Immediately stop using the DURAMAX Stacked Tip 28cm kit if you have it.
No, the product may contain metal shavings that could cause serious complications requiring surgery.
Stop using it immediately and contact Angiodynamics for further instructions.
Look for product number H787103028041 or lot number 5805840 on the kit.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1768-2024 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1768-2024 from Angiodynamics. 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.
