Z-2453-2024 Class II Ongoing

Recalled by Angiodynamics, Inc. — Queensbury, NY

Recall Details

Product Type
Devices
Report Date
August 7, 2024
Initiation Date
June 18, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
519 boxes

Product Description

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

Reason for Recall

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)

Distribution Pattern

US Nationwide distribution.

Code Information

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