Z-0304-2017 Class II Terminated
FDA device recall Z-0304-2017 was initiated by Nova Ortho-Med Inc on October 1, 2016 and is designated Class II. 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 of… The recall status is terminated (terminated February 6, 2017). Affected quantity: 1,380 units.
Recall Details
- Product Type
- Devices
- Report Date
- November 2, 2016
- Initiation Date
- October 1, 2016
- Termination Date
- February 6, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,380 units
Product Description
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.
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
Code Information
Serial No. YA 4205RDFG004 TO YA4205RDFG0098 YZ4205BKFC0002 TO YZ4205RDFE0100