Class II
Medical Device Recall: Optical Inspection System, YSi series, YRi series. Affected models: YSi-V, YSi-V(HS2), YRi-V
YAMAHA MOTOR CORPORATION · April 17, 2024
Reason for Recall
Non-medical laser products which were determined to not be in compliance with 21 C.F.R. ¿ 1010.2 in that they currently do not bear the required certification label.
Distribution
US Nationwide
States Affected
NATIONWIDE
Quantity Affected
67
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1816-2024
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.