FDA Medical Device Recalls (openFDA)
Codman & Shurtleff Inc: GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm).
- Recall number
- Z-2280-2019
- Recalling firm
- Codman & Shurtleff Inc
- Product
- GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm).
- Status
- Terminated
- Initiated
- 2019-05-16
- Posted
- not on file
- Terminated
- 2020-06-04
- Reason
- Incorrect coil length on the label
- Root cause
- Error in labeling
- Action
- Sales representatives will communicate the action to be taken with respect to this recall. If you have additional questions about this action, please contact y0ur local customer service.
- Quantity
- 28 units
- Distribution
- Japan
- Lot, serial or model codes
- Lot/Serial No: L14364 UDI:10886704080138
- 510(k) numbers
- ["K171862"]
- PMA numbers
- not on file
- Product code
- HCG
- Firm FEI
- 3013875781
- Firm city
- Fremont
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28