Yamaha Motor Corporation is recalling 443 non-medical laser products, including various Surface Mounter and Optical Inspection systems, because they are missing required FDA certification labels. These industrial machines, which include models from the YR, YS, i-Pulse, Sigma, and YSi series, do not comply with federal safety standards regarding laser product labeling. Consumers should contact Yamaha to ensure their equipment receives the necessary safety certification markings.
The absence of required certification labels means the equipment does not meet federal safety standards for laser products, which are intended to inform users of potential laser radiation hazards and ensure the device operates within regulated safety parameters.
Certification labeling update
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.