Apic Yamada America is recalling 6 units of its WCM series molding equipment, specifically model WCM-330GL-i. These products were distributed without a required label that certifies compliance with FDA electronic product regulations. While no injuries or incidents have been reported, this equipment must have the proper labeling to ensure it meets federal safety standards for electronic products. Owners should contact Apic Yamada America to arrange for the necessary corrections to their equipment.
The missing labels indicate that the equipment has not been verified to meet specific FDA safety requirements for electronic products. This lack of compliance could mean the equipment poses unknown operational risks, though no injuries have been reported to date.
Recall number Z-2150-2025. Quantity: 6 units.
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
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