Recall Z-1430-2009 ยท FPA Set, Administration, Intravascular
B. Braun Medical, Inc.
Ultrasite IV Administration Set with Universal Spike, three Backcheck Valves, three Ultrasite Injection Sites and Spin-Lock Connector, Catalog #470007. For use with Secondary Container.
| Date | Jun 5, 2009 (initiated Mar 27, 2009) |
| Status | Terminated |
| Reason | Device defect is occlusion/no flow. |
| Root cause | Mixed-up of materials/components |
| Action | An Urgent - Medical Device Recall notice was issued via US Postal Service Certified Mail with registered return receipt mail or FedEx to all customer/distributors in receipt of affected product on 3/27/09. Direct customers received letters addressed to Materials Management that informed them of this recall and provided instructions for disposition of affected product in their inventory. Distributors received the direct customer recall letter along with a cover letter outlining their responsibilities to execute the recall and notify their customers as requested. Distributors are to immediate |
| Quantity | 50 units |
| Distribution | Worldwide Distribution -- USA and Canada. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K955585 | V2 INJECTION SITE B.Braun Medical, Inc., May 15, 1996 |