4205 Journey Rolling Walker Product Usage: used to assist people in… — Class II medical device recall Z-0304-2017
Terminated recall by Nova Ortho-Med Inc, reported 2016-11-02, distributed nationwide. Nova Medical is recalling the Journey Rolling Walker because the screws used to hold the black side support pi
| Recall number | Z-0304-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nova Ortho-Med Inc, Carson, CA, United States |
| Recall initiated | 2016-10-01 |
| Classified | 2016-10-24 |
| Reported by FDA | 2016-11-02 |
| Terminated | 2017-02-06 |
| Distributed | Nationwide (US) |
| Quantity | 1,380 units |
| Serial numbers | 4205RDFG004, YA4205RDFG0098, YZ4205BKFC0002, YZ4205RDFE0100 |
Product
4205 Journey Rolling Walker Product Usage: used to assist people in walking
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0304-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.