Angiodynamics recalls SOFT-VU KUMPE 5F X 65CM catheters due to potential mislabeling of inner pouch. This may cause incorrect catheter length use in medical procedures. Affected units have specific catalog and lot numbers.
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 recalls certain SOFT-VU KUMPE 5F X 65CM 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, which might cause complications.
The inner pouch label may show a different catheter model than the box label. This could lead to using the wrong catheter length during medical procedures, potentially causing complications.
Healthcare providers using these catheters for angiographic procedures are most at risk. Patients receiving the catheters could be affected if the wrong length is used.
Check the box label for catalog number 10732701 and lot number A0424031. The inner pouch label may show a different model or length than the box.
Compare the inner pouch label with the box label to ensure they match the correct catheter length.
The recall is due to potential mislabeling, not inherent danger. Using the correct catheter length as labeled should be safe.
Check the box label for catalog number 10732701 and lot number A0424031. The inner pouch label may show a different model than the box.
No action is required if the labels match. Only check labels to ensure correct catheter length is used.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2454-2024 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2454-2024 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.
