Class II
Medical Device Recall: Cascade IOMAX Cortical Module, REF: 190296-200
Cadwell Industries Inc · May 17, 2024
Reason for Recall
Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.
Distribution
US: IL CA OUS: Canada, Germany, India, Italy, Mexico, Poland, South Africa, Spain, Taiwan, United Kingdom
States Affected
CA, IL
Quantity Affected
26 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2349-2024
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.