Recall Z-0304-2017— Nova Ortho-Med Inc
Class II · Terminated
Class II FDA medical device recall by Nova Ortho-Med Inc, initiated 2016-10-01, terminated 2017-02-06. FDA's recall record names no specific 510(k) clearance for this event. Product: 4205 Journey Rolling Walker Product Usage: used to assist people in walking. 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..
- Recalling firm
- Nova Ortho-Med Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-10-01
- Terminated
- 2017-02-06
- Firm location
- Carson, CA, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.