SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702
FDA Recall Z-2453-2024 · Posted 2024-07-31
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Recalling FirmAngiodynamics, Inc.
Recall StatusOpen, Classified
Product CodeDQO
Date Initiated2024-06-18
Product Quantity519 boxes
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)
Firm Action
Angiodynmaics issued Urgent Medical Device Recall Letter on 6/18/24 via Federal Express to end-users. Letter states reason for recall, health risk and action to take:
" IMMEDIATELY
o Stop using the product subject to recall.
o Remove any affected (recalled) product from your inventory (whether in labs, Central
Supply, Shipping and Receiving or ANY other location).
o Segregate this product in a secure location for return to AngioDynamics, Inc.
o Forward a copy of this recall notification to all sites to which you have distributed affected product.
2. Complete and return the Reply Verification Tracking Form.
Promptly complete, sign, and return the enclosed Reply Verification Tracking Form (even if you do not have any product to return); following the directions on this page and the Reply Verification Tracking Form.
Email Reply Verification Tracking Form (preferred): [email protected]
Fax Reply Verification Tracking Form:
Attn: Soft-Vu Kumpe Recall Coordinator
Fax number 1-855-273-0519
" Call AngioDynamics Customer Service at 1-800-772-6446 between 8:00 a.m. and 6:00 p.m. (Monday Friday: Eastern Standard Time) to obtain a replacement or credit for your returned product.
" Report any Adverse reactions or quality problems associated with recalled devices to US FDA via MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
3. Package and Return the Recalled Product.
" Package any product that is being returned in an appropriate shipping box.
" Write the RMA number on the RMA/Address label (provided on the Recall Verification Tracking Form) and affix the label to the outside of the shipping box.
" Seal the box and return to:
AngioDynamics, Inc.
24 Native Drive
Queensbury, NY 12804
Attn: Soft-Vu Kumpe Recall Coordinator
Root Cause
Packaging change control
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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