Class II
Medical Device Recall: O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
Emergency Products & Research · February 27, 2024
Reason for Recall
Failure of adhesive to secure the pole insert.
Distribution
US Nationwide distribution in the states of CA, CO, FL, GA, IL, IN, KS, MA, MI, NJ, NY, OH, OK, PA, SC, TX, UT, VA, WA.
States Affected
NATIONWIDE
Quantity Affected
190,000 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1395-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.