FDA Device recall Z-2280-2019
GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm)
- FDA Device
- Class II
- terminated
- Published 2019-08-21
On 2019-08-21 the FDA classified a Class II recall of GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm) by Codman And Shurtleff, citing incorrect coil length on the label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2280-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-05-16 |
| Published | 2019-08-21 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Codman And Shurtleff |
| Distribution | n/a |
Product
GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm).
Reason
Incorrect coil length on the label
Identifiers
| code_info | Lot/Serial No: L14364 UDI:10886704080138 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2280-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.