---
title: "AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System ... — FDA record Z-1261-2022 | Is It on Recall"
description: "Due to incorrect size and configuration labeling of the detachable coil system."
url: https://isitonrecall.com/recall/fda-device-z-1261-2022-axium-detachable-coil-system-ref-qc-4-12-helix-axium-detachable-coil-system-ref-qc-10-30-3d/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D; — FDA record Z-1261-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 27, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;
- **Reason**: Due to incorrect size and configuration labeling of the detachable coil system.
- **Classification**: Class II
- **Recalling firm**: Micro Therapeutics, Inc.
- **Quantity**: 96 systems
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1261-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1261-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Product Number: QC-4-12-HELIX UDI-DI (GTIN) Code: 00847536029590 Lot Number: B240079 Product Number: QC-10-30-3D UDI-DI (GTIN) Code: 00847536030138 Lot Number: B240084 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

International distribution in the countries of China and Republic of Korea.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jun 22, 2022
- **Recall initiation date**: Apr 27, 2022
- **Center classification date**: Jun 13, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1261-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Micro Therapeutics, Inc. records](https://isitonrecall.com/brand/micro-therapeutics-inc/)