Device recall
Z-1173-2024: OPTIMIZER model CCM X11 implantable pulse generator (IPG) devices - Smart Mini…
FDA device recall · Class II · IMPULSE DYNAMICS (USA) INC
Key facts
| Recall number (Z-number) | Z-1173-2024 |
|---|---|
| Recall event | 93791 |
| Product | OPTIMIZER model CCM X11 implantable pulse generator (IPG) devices - Smart Mini and Lite |
| Product code | QFV |
| Recalling firm | IMPULSE DYNAMICS (USA) INC |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P180036, P180036S007, P180036S021, P180036S025 |
| FEI number | 3017555074 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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