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Open, Classified

Molding Equipment. WCM series. Model WCM-330GL-i

FDA Recall Z-2150-2025 · Posted 2025-07-31

Recalling FirmApic Yamada America
Recall StatusOpen, Classified
Product CodeRHK
Date Initiated2025-04-07
Product Quantity6

Reason for Recall

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.

Firm Action

Apic Yamada Corporation (AYC) sends notification letters to customers and provides the following information including affected product description, details on the issue and Corrective Action Instructions To complete the remediation of affected products, the our FSE will follow these steps: 1. Please locate the certification labels provided in this packet. 2. Following the label placement instructions for your product found below, affix the label in the indicated position.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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