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Recall Observatory FDA recall evidence

Device product

4205 Journey Rolling Walker Product Usage: used to assist people in walking

Z-0304-2017

October 01, 2016

Class II

Product summary

Firm
Nova Ortho-Med Inc
Event
Event 75408
Status
Terminated
Classification
Class II
Quantity
1,380 units
Official record key
device-enforcement:Z-0304-2017

Official wording

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.

Code information: Serial No. YA 4205RDFG004 TO YA4205RDFG0098 YZ4205BKFC0002 TO YZ4205RDFE0100

Distribution pattern: 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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.