Angiodynamics recalls DURAFLOW 2 24cm Straight Basic Kit for hemodialysis access due to potential metal shavings that could cause surgical removal. Affected units 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 DURAF: 2 24cm Straight Basic Kit for hemodialysis vascular access because it may contain metal shavings that could travel to the bloodstream and require surgery. This is a serious risk for patients needing long-term dialysis access.
The Tri-Ball Tunneler component may have metal shavings that can become dislodged and travel through the bloodstream. This could lead to embolism, requiring surgical intervention to remove the shavings.
Patients using this kit for hemodialysis or apheresis treatments are most at risk. The product is designed for long-term vascular access in dialysis patients.
Check for product number H787103012015 and lot numbers 5807192 or 5807197 on the kit packaging. The product is intended for hemodialysis and apheresis vascular access.
Immediately stop using the DURAFLOW 2 24cm Straight Basic Kit if it has the product number H787103012015 and lot numbers 5807192 or 5807197.
The recall is for specific units that may contain metal shavings; the kit is generally safe but affected units require immediate action.
Stop using it immediately and contact Angiodynamics for guidance on next steps.
Look for product number H787103012015 and lot numbers 5807192 or 5807197 on the packaging.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1760-2024 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1760-2024 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.
