Recall Z-1221-2020 ยท KRD Device, Vascular, For Promoting Embolization
Microvention, Inc.
Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil, REF numbers 45-681026, 45-681434, 45-682050, and 45-680820, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.
| Date | Nov 24, 2019 |
| Status | Terminated |
| Reason | The devices may be missing the implant coil. |
| Root cause | Other |
| Action | The recalling firm issued emails dated 11/24/2019 to the Terumo distributors and provided instructions for notification of their customers (physicians). |
| Quantity | 107 units |
| Distribution | The devices were distributed to Maryland. There was no direct military/government distribution. Foreign distribution was made direct to Belgium, Japan, Australia, Argentina, and Mexico. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K120630 | AZUR DETACHABLE 18 MicroVention, Inc., Mar 28, 2012 |