Recall Z-1818-2019 ยท PND Midline Catheter
Arrow International Inc
Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS
| Date | Apr 23, 2019 |
| Status | Terminated |
| Reason | Lidstock states the incorrect expiration date for the product |
| Root cause | Process control |
| Action | Arrow International initiated recall by letter dated April 23,2019 described the problem, health risk and action to take: If you have affected stock in inventory, immediately discontinue use and quarantine the products. 2. Complete the enclosed Acknowledgement Form indicating whether you do or do not have stock and fax it to 1-855-419-8507 or email to recalls@teleflex.com. A customer service representative will contact you with a Return Goods Authorization (RGA) number and provide instructions for the return of products. Distributors requested to subrecall. Questions, contact your local sale |
| Quantity | 430 units |
| Distribution | Nationwide Foreign: |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K161313 | ARROW Pressure Injectable Midline Catheter with Chlorag+ard Antimicrobial and Antithrombogenic Technology Arrow International, Inc. (Subsidiary of Teleflex, Inc.), Aug 24, 2016 |