# FDA recall Z-2280-2019

> **Codman & Shurtleff Inc** · Class II · device recall initiated 2019-05-16.

## Product

GALAXY G3 Mini Microcoil Delivery System  Product No: GLM915030 (3 cm).

## Reason for recall

Incorrect coil length on the label

## Distribution

Japan

## Key facts

- **Recall number:** Z-2280-2019
- **Recalling firm:** Codman & Shurtleff Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-16
- **Report date:** 2019-08-21
- **Termination date:** 2020-06-04

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2280-2019

## Citation

> AI Analytics. FDA recall Z-2280-2019. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-2280-2019. Source: US FDA. Licensed CC0.

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