Drug recall
GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm).
FDA recall event 83502 · Class II · Codman & Shurtleff Inc
Key facts
| Event ID | 83502 |
|---|---|
| Recall numbers | Z-2280-2019 |
| Recalling firm | Codman & Shurtleff Inc |
| Product type | Devices |
| Products | GALAXY G3 Mini Microcoil Delivery System Product No: GLM915030 (3 cm). |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect coil length on the label |
| Initiation date | May 16, 2019 |
| Report date | Aug 21, 2019 |
| Termination date | Jun 4, 2020 |
| City | Fremont |
| State | CA |
| Country | United States |
| FEI number | 3013875781 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: