Recall Z-2492-2010 ยท DQY Catheter, Percutaneous
Arrow International Inc
Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter, ARROW g+ard Blue Catheter
| Date | Sep 25, 2010 (initiated Jul 29, 2010) |
| Status | Terminated |
| Reason | Incorrectly assembled 18 Ga x 2 1/2 Introducer Needle |
| Root cause | Mixed-up of materials/components |
| Action | The recalling firm issued an Urgent Medical Device Recall letter dated 7/23/2010 along with a a recall acknowledgement and stock status form. |
| Quantity | 2 |
| Distribution | The product was shipped to medical centers and hospitals nationwide and to Australia, New Zealand, and Europe. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K820648 | ARROW M.I.S. MULTI-LUMEN CATHETERIZA Arrow Intl., Inc., Apr 14, 1982 |