Lower riskMedical device recall · FDA · Published June 18, 2024
Angiodynamics SOFT-VU KUMPE 5F X 40CM: Mislabeled Inner Pouch Warning
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)
Take action
Contact the company
📍Recalling firmAngiodynamics, Inc.603 Queensbury Ave · Queensbury, NY 12804-7619
“Angiodynamics SOFT-VU KUMPE 5F X 40CM: Mislabeled Inner Pouch Warning.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54791-angiodynamics-soft-vu-kumpe-5f-x-40cm-mislabeled-inner-pouch. Based on FDA recall #Z-2453-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2453-2024%22&limit=1).
The FDA announced on June 18, 2024, that Angiodynamics, Inc. is recalling SOFT-VU KUMPE 5F X 40CM catheters due to mislabeled inner pouches. The hazard involves potential confusion regarding catheter length because the inner label may contain information for a different model.
How to tell if you have it
Brand: Angiodynamics
Product: SOFT-VU KUMPE 5F X 40CM
Catalog Number: 10732702
UPN: H787107327025 (Box) / 15051684009782 (Pouch)
Lot Number: A0424035
The hazard
According to the FDA, the inner pouch label for the recalled devices may contain information for a different model, specifically regarding catheter length. The shelf-box labeling remains accurate for the packaged devices.
Context
GovInfoNow's records show Angiodynamics, Inc. has had 18 other recalls on record since June 5, 2017. Other recent recalls of similar products include Bard Safe-T-Centesis 6 Fr Catheter Drainage Tray Recall (Nov. 6, 2025) and BD InLay Optima Ureteral Stent Kit: Labeling Discrepancy Risk (Nov. 6, 2025).
How to tell if you have this one
Check the box label for catalog number 10732702. The inner pouch label has a different catalog number (15051684009782) than the box (10732702).
Brand
Angiodynamics
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution.
Recall number
Product, codes & lots
Quantity
Z-2453-2024
SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702; UPN: H787107327025 UDI-DI: 25051684009789 (Box) 15051684009782 (Pouch) Lot Number: A0424035
519 boxes
Z-2454-2024
SOFT-VU KUMPE 5F X 65CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732701; UPN: H787107327015 UDI-DI: 25051684009772 (Box) 15051684009775 (Pouch) Lot Number: A0424031
595 boxes
Based on the official FDA remedy
What to do — step by step
Check Box Label
Look for catalog number 10732702 on the box label to confirm the product.
Verify Pouch Label
Ensure the inner pouch label shows catalog number 15051684009782, which matches the box.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 50 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2453-2024 (June 18, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2453-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.