FDA Device recall Z-0944-2018
ReWalk Personal 6.0. Catalog number: 50-20-0004
- FDA Device
- Class II
- terminated
- Published 2018-03-21
On 2018-03-21 the FDA classified a Class II recall of ReWalk Personal 6.0. Catalog number: 50-20-0004 by Argo Medical Technologies, citing firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0944-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-08-14 |
| Published | 2018-03-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Argo Medical Technologies |
| Distribution | n/a |
Product
ReWalk Personal 6.0. Catalog number: 50-20-0004.
Reason
Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
Identifiers
| code_info | Date range of Distribution: 09/01/2015 to 09/06/2017. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0944-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.