Medical Device Recall: Mint Lesion; Software Versions: 3.4.0 up to 3.9.5.;
Mint Medical GmbH · January 7, 2026
Reason for Recall
If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to other patients.
Distribution
Worldwide distribution - US Nationwide and the countries of Germany, Switzerland, Austria, Belgium, Italy, France, Romania, Netherlands, United Kingdom, Spain, Czech Republic, Ireland, Poland;
States Affected
NATIONWIDE
Quantity Affected
101 systems
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2068-2026
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.