Class II
Medical Device Recall: CMS8000 Patient Monitor
Contec Medical Systems Co., Ltd. · April 10, 2025
Reason for Recall
Patient monitor has nine identified cybersecurity vulnerabilities.
Distribution
US Nationwide distribution in the states of CA, IL, FL, KY, TX.
States Affected
NATIONWIDE
Quantity Affected
7773
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1764-2025
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.