Microvention, Inc. Recall: Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil,
Microvention, Inc. Recall: Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Microvention, Inc.; Product: Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-751324, 45-751632, 45-752039,
| Recalling firm | Microvention, Inc. |
|---|---|
| Product | Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-751324, 45-751632, 45-752039, 45-750407, 45-750511, 45-750617, 45-750609, 45-750812, 45-750824, MV-AX50407CD, MV-AX50511CD, MV-AX50617CD, MV-AX50824CD, and MV-AX51019CD, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica. |
| Reason for recall | The devices may be missing the implant coil. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| 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. |
| Recall initiated | 20191124 |
| Recall number | Z-1225-2020 |
| Category | device |
| State | CA |
| Country | United States |
$29/mo
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