Angiodynamics recalls SOFT-VU KUMPE 5F X 40CM catheters due to potential mislabeling of inner pouch. This may cause incorrect catheter length use in angiographic procedures. Check your box and pouch labels for catalog number 10732702.
Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)
Angiodynamics is recalling SOFT-VU KUMPE 5F X 40CM catheters because the inner pouch label might show a different model than the box. This could lead to using the wrong catheter length during medical procedures.
The inner pouch label may show a different catheter model than the box label. This could result in using the wrong catheter length during medical procedures, but it does not cause immediate harm.
Healthcare professionals using these catheters for angiographic procedures. Patients receiving the catheters are at low risk since the issue is labeling, not a physical hazard.
Check the box label for catalog number 10732702. The inner pouch label has a different catalog number (15051684009782) than the box (10732702).
Look for catalog number 10732702 on the box label to confirm the product.
Ensure the inner pouch label shows catalog number 15051684009782, which matches the box.
No, this is a labeling issue that could lead to using the wrong catheter length, but it does not cause immediate harm.
Check the box label for catalog number 10732702. The inner pouch label should show catalog number 15051684009782.
No, you can continue using it as long as you verify the labels match.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2453-2024 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2453-2024 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.
