Class II
Medical Device Recall: TMJ Bilateral Implants, REF: CHG020
TMJ Solutions Inc · February 11, 2026
Reason for Recall
Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.
Distribution
US Nationwide distribution in the state of MA.
States Affected
NATIONWIDE
Quantity Affected
1
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2524-2026
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.