Xcela PICC with PASV Valve Technology/Kit 5 F-55cm; (Maximum Flow Rate 3.5 mL/Sec)-indicated for short or long-term peripheral access to the central venous system for intravenous therapy, including but not limited to, the administration of fluids, medications, and nutrients; the sampling of blood; and for power injection of contrast media. Catalog Number: 60M701995
FDA Recall Z-2617-2021 · Posted None
Advertisement
Recalling FirmAngiodynamics Inc. (Navilyst Medical Inc.)
Recall StatusTerminated
Product CodeN/A
Date Initiated2017-10-17
Date Terminated2022-06-14
Product Quantity4 boxes (5/each)= 20 eaches
Reason for Recall
Mislabeled: The product is labeled as 5F (55cm; Maximum Flow Rate 3.5 mL/Sec) and the product is actually 4F (55cm; Maximum Flow Rate 3.5 mL/Sec).
Firm Action
Angiodynamics issued Recall Notifications Packages via Federal Express to 1 International Medical Facility on 2017-10-17. Letter states reason for recall, health risk and action to take:
IMMEDIATELY " Stop using the product subject to recall.
" Remove any affected (recalled) product from your inventory (whether in labs, Central
Supply, Shipping and Receiving or ANY other location).
" Segregate this product in a secure location for return to AngioDynamics, Inc.
" Forward a copy of this recall notification to all sites to which you have distributed affected product.
Complete and return the Reply Verification Tracking Form.
" If affected product is located in your institution, please can AngioDynamics Customer Service at 1-800-772-6446 between 8:00 a.m. and 7:00 p.m. (Monday - Friday: Eastern Standard Time) to obtain a replacement or credit for your returned product.
" 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.
o Email Reply Verification Tracking Form (preferred): [email protected]
o Fax Reply Verification Tracking Form:
Ann: PICC Kit Product Description Recall Coordinator
Fax number 1 800-782-1357.
Root Cause
Error in labeling
Distribution Pattern
Canada
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement