GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 — Class II medical device recall Z-2280-2019
Terminated recall by Codman & Shurtleff Inc, reported 2019-08-21. Incorrect coil length on the label
| Recall number | Z-2280-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Codman & Shurtleff Inc, Fremont, CA, United States |
| Recall initiated | 2019-05-16 |
| Classified | 2019-08-15 |
| Reported by FDA | 2019-08-21 |
| Terminated | 2020-06-04 |
| Countries outside the US | JP |
| Quantity | 28 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 10886704080138 |
| Serial numbers | L14364 |
Product
GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm).
Reason for recall
Incorrect coil length on the label
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2280-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.