Fremont, CA, United States
Codman & Shurtleff Inc recalls
1 recall recorded since 2018, most recently on 16 May 2019. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 16 May 2019
- Terminated
- 4 June 2020
- Reason
- Incorrect coil length on the label
- Distribution
- Japan
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2280-2019
- GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm).
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.