Device recall
Z-0944-2018: ReWalk Personal 6.0. Catalog number: 50-20-0004.
FDA device recall · Class II · Argo Medical Technologies Ltd
Key facts
| Recall number (Z-number) | Z-0944-2018 |
|---|---|
| Recall event | 79186 |
| Product | ReWalk Personal 6.0. Catalog number: 50-20-0004. |
| Product code | PHL |
| Recalling firm | Argo Medical Technologies Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 12, 2019 |
| 510(k) numbers | K131798 |
| FEI number | 3007615665 |
At a glance
- 1–9 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