AMICUS Exchange Kit; Product Usage: This kit is designed for use with the AMICUS separator for the Therapeutic Plasma Ex
FDA device recall Z-1523-2013 · posted 2013-06-08 · Terminated
Recall details
- Recalling firm
- Fenwal Inc
- 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
- 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.
- Root cause
- Process change control
- Status
- Terminated
- Product code
- LKN
- Quantity affected
- 19 Cases (114 Units)
- Distribution
- USA Nationwide Distribution
- Date initiated
- 2013-05-24
- Date posted
- 2013-06-08
- Date terminated
- 2016-08-01
- Location
- Lake Zurich, IL
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| AMICUS SEPARATOR SYSTEM- USE IN THERAPEUTIC PLASMA EXCHANGE AND FILTER SET FOR AMICUS TPE (K111702) | Fenwal, Inc. | 2012-03-22 |