Device recall
Z-2825-2018: Sorin Platinium CRT-D 1741 DF-4, Sterile EO. Implantable Cardiac Defibrillator…
FDA device recall · Class II · Sorin CRM SAS
Key facts
| Recall number (Z-number) | Z-2825-2018 |
|---|---|
| Recall event | 80636 |
| Product | Sorin Platinium CRT-D 1741 DF-4, Sterile EO. Implantable Cardiac Defibrillator and Resynchronization Therapy Defibrillator |
| Product code | NIK |
| Recalling firm | Sorin CRM SAS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 6, 2024 |
| PMA numbers | P060027, P060027S079 |
| FEI number | 3008159616 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database