# FDA recall Z-1222-2020

> **Microvention, Inc.** · Class II · device recall initiated 2019-11-24.

## Product

Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers 45-781032, 45-781238, 45-781434, 45-781639, 45-781836, 45-782040, 45-780202, 45-780204, 45-780304, 45-780308, 45-780413, 45-780516, 45-780620, 45-780724, 45-780828, 45-780928, MV-AX80202CL, MV-AX80204CL, MV-AX80304CL, MV-AX80308CL, MV-AX80413CL, MV-AX80516CL, MV-AX80620CL, MV-AX80724CL, MV-AX80828CL, MV-AX80928CL, MV-AX81032CL, MV-AX81238CL, MV-AX81434CL, MV-AX81639CL, and MV-AX82040CL, 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.

## 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.

## Key facts

- **Recall number:** Z-1222-2020
- **Recalling firm:** Microvention, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-11-24
- **Report date:** 2020-02-19
- **Termination date:** 2021-04-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Aliso Viejo, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1222-2020

## Citation

> AI Analytics. FDA recall Z-1222-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1222-2020. Source: US FDA. Licensed CC0.

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