Class II
Medical Device Recall: GM60A. Digital Diagnostic Mobile X-Ray System.
NeuroLogica Corporation · July 8, 2024
Reason for Recall
Potential for the anti-fall system of the device arm to fail.
Distribution
US Nationwide distribution in the states of AR, CT, GA, IN, KS, MA, MD, MO, MS, NC, ND, NJ, NV, OH, PA, VA, WV & DC.
States Affected
NATIONWIDE
Quantity Affected
31 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2715-2024
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.