Angiodynamics recalls DURAMAX VASC-PAK catheters due to potential metal shavings that could cause embolism requiring surgery. Affected units have specific 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 DURAM:MAX VASC-PAK catheters that may contain metal shavings. These shavings could travel to the bloodstream and cause serious complications needing surgery.
The catheter's Tri-Ball Tunneler component may have loosely attached metal shavings. If these shavings enter the bloodstream, they could cause blockages or require surgical removal.
Hemodialysis and apheresis patients using the DURAMAX VASC-PAK catheters are most at risk. The recall affects specific lot numbers of the product.
Check for lot number 5809464 on the product label. The DURAMAX STACKED TIP 32 CM STRAIGHT VASC-PAK catheters are used for long-term vascular access in hemodialysis and apheresis.
Look for lot number 5809464 on the catheter label to confirm if it's affected.
The Tri-Ball Tunneler may contain loosely affixed metal shavings that could embolize and require surgical removal.
Check the product label for lot number 5809464. If affected, contact Angiodynamics for guidance.
The product may contain metal shavings that could cause serious complications, so affected units should be checked.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1773-2024 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1773-2024 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.