Class II
Medical Device Recall: Lactose Intolerance Test
GET TESTED INTERNATIONAL AB · November 3, 2025
Reason for Recall
Distribution without premarket approval/clearance.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
15 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0786-2026
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.