Skip to content
Recall Observatory FDA recall evidence

Device product

SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702

Z-2453-2024

June 18, 2024

Class II

Product summary

Firm
Angiodynamics, Inc.
Event
Event 94903
Status
Ongoing
Classification
Class II
Quantity
519 boxes
Official record key
device-enforcement:Z-2453-2024

Official wording

Reason: 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)

Code information: UPN: H787107327025 UDI-DI: 25051684009789 (Box) 15051684009782 (Pouch) Lot Number: A0424035

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Mislabeled