Medical device recalls Moderate risk

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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