Angiodynamics recalls DURAMAX Stack Tip kits for possible metal shavings that could cause embolism requiring surgery. Affected kits have specific product numbers and lot numbers.
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 kits used for hemodialysis and apheresis 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.
The Tri-Ball Tunneler component may have metal shavings that can become loose and enter the bloodstream. This could cause a blockage requiring surgical intervention to remove the shavings.
Patients using hemodialysis or apheresis treatments with the recalled DURAM:MAX Stack Tip kits are most at risk. The recall affects specific product numbers and lot numbers.
Check for product number H787103028055 and lot number 5809646 on the kit. The DURAMAX Stack Tip kit is used for long-term vascular access in hemodialysis and apheresis treatments.
Immediately stop using the DURAMAX Stack Tip kit if it has product number H787103028055 and lot number 5809646.
The Tri-Ball Tunneler may contain loosely affixed metal shavings that could embolize and require surgical removal.
Stop using it immediately and contact Angiodynamics for instructions.
No, the kit is not safe to use as it may contain metal shavings that could cause serious health risks.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1770-2024 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1770-2024 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.
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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.
