Apic Yamada America recalls WCM-330GL-i molding equipment due to missing FDA label. This may violate electronic product regulations. No action is required as the product is not in use.
Apic Yamada has recently discovered that certain products may be out of compliance with FDA electronic product regulations in that they did not bear a required label.
Apic Yamada America is recalling their WCM-330GL-i molding equipment because it lacks a required FDA label. This issue does not pose a safety risk but violates electronic product regulations.
The equipment may not have a required FDA label, which is a regulatory compliance issue. This does not cause physical harm but violates electronic product regulations. The hazard is not a safety risk but a legal compliance problem.
Users of the WCM-330GL-i molding equipment who purchased it from Apic Yamada America. The risk is minimal as the product is not in use and the issue is regulatory compliance.
Check for the model number WCM-330GL-i on the equipment. The product was sold by Apic Yamada America and is part of the WCM series. No specific date or location is mentioned in the recall.
Look for the required FDA label on the equipment. If missing, the product is part of the recall.
No, the product is not dangerous. The issue is a missing FDA label, which is a regulatory compliance problem, not a safety hazard.
No action is required as the product is not in use and the issue is regulatory compliance.
Check for the model number WCM-330GL-i on the equipment. The product was sold by Apic Yamada America and is part of the WCM series.
We’ve drafted a message you can send Apic Yamada America to request your refund or repair — edit it as you like.
Subject: Recall Z-2150-2025 — Apic Yamada America Apic Yamada America Hello, I own a Apic Yamada America that is covered by recall Z-2150-2025 from Apic Yamada America. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
