FDA Device recall Z-0304-2017
4205 Journey Rolling Walker Product Usage: used to assist people in walking
- FDA Device
- Class II
- terminated
- Published 2016-11-02
On 2016-11-02 the FDA classified a Class II recall of 4205 Journey Rolling Walker Product Usage: used to assist people in walking by Nova Ortho Med, citing nova Medical is recalling the Journey Rolling Walker because the screws used to hold the black side support pieces to the frame can become loose over time. This can result in the….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0304-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-10-01 |
| Published | 2016-11-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Nova Ortho Med |
| Distribution | US |
Product
4205 Journey Rolling Walker Product Usage: used to assist people in walking
Reason
Nova Medical is recalling the Journey Rolling Walker because the screws used to hold the black side support pieces to the frame can become loose over time. This can result in the locking nut coming off and the screw falling out.
Identifiers
| code_info | Serial No. YA 4205RDFG004 TO YA4205RDFG0098 YZ4205BKFC0002 TO YZ4205RDFE0100 |
|---|
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-0304-2017%22
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