Nova Ortho-Med Inc recalls 4205 Journey Rolling Walker Product Usage: used to assist people in walking
- Recall date
- October 1, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0304-2017
- FDA classification
- Class II
- Brand / firm
- Nova Ortho-Med Inc
- Sold / distributed
- 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
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
4205 Journey Rolling Walker Product Usage: used to assist people in walking
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