RecallDepth

AMICUS Exchange Kit; Product Usage: This kit is designed for use with the AMICUS separator for the Therapeutic Plasma Exchange (TPE) procedure. Sterilized by irradiation. Sterile fluid path. Non-pyrogenic fluid path.

Company
Fenwal Inc
Recall Initiated
May 24, 2013
Posted
June 8, 2013
Terminated
August 1, 2016
Recall Number
Z-1523-2013
Quantity
19 Cases (114 Units)
Firm Location
Lake Zurich, IL

Reason for Recall

Fenwal has initiated a voluntary Urgent Product Recall for lot FA12C07070 of product code R4R2339, Amicus Exchange Kits. Fenwal identified a labeling issue with this batch of Product Code R4R2339 (which was cleared for European use only) in which this batch was distributed within the United States market. The problem is identified as labeling that did not include the written description for the s

Distribution

USA Nationwide Distribution

Lot / Code Info

Model No.: R4R2339;  Lot No.: FA12C07070;  Expiration Date: 03/2014

Root Cause

Process change control

Action Taken

Fenwal sent an Urgent Product Recall letter dated May 24, 2013 to all affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to immediately check inventory, discontinue the use of this prod.uct, return the affected product to Fenwal, and complete and return the attached reply form. For questions call 1-800-333-6925.

More recalls by Fenwal Inc

View all recalls by this company →