Device recall
Z-1139-2026: Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait…
FDA device recall · Class II · Community Products, LLC
Key facts
| Recall number (Z-number) | Z-1139-2026 |
|---|---|
| Recall event | 98140 |
| Product | Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion. |
| Product code | FSA |
| Recalling firm | Community Products, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1319061 |
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