Medical Device Recalls
-
|
1 to 3 of 3 Results
Related Medical Device Recalls |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Z-3081-2026 - LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS US, Model Number 7260, All Versions (Current 7.8) | 2 | 09/02/2026 |
FEI # 2124215 Boston Scientific Corporation |
| Z-3083-2026 - LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS ANZ, Model Number 7248, All Versions (Current 7.7) | 2 | 09/02/2026 |
FEI # 2124215 Boston Scientific Corporation |
| Z-3082-2026 - LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS EU, Model Number 7246, All Versions (Current 7.7) | 2 | 09/02/2026 |
FEI # 2124215 Boston Scientific Corporation |
-







