Class II — Nova Ortho-Med Inc
| Recalling firm | NOVA ORTHO-MED, INC. |
|---|---|
| Registered facility | NOVA ORTHO-MED, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| 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. |
| Product | 4205 Journey Rolling Walker Product Usage: used to assist people in walking |
| Quantity | 1,380 units |
| Distribution | US Nationwide Distribution in the states of: CA, IN, HI, CT, UT, WA, FL, VA, WI, OH, MN, KS, MD, IL, MO, WY, MT, ME, PA, TN, MI, OR, NY, NJ, ID, NC, IA, OK, AR, VT, SC, TX |
| Initiated | 2016-10-01 |
| Classified | 2016-10-24 |
| Terminated | 2017-02-06 |
| Recall number | Z-0304-2017 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Nova Ortho-Med Inc (Z-0304-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/75408/
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