Apic Yamada America: Device Recall
Recall #Z-2150-2025 · 04/07/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2150-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Apic Yamada America
- Status
- Ongoing
- Date Initiated
- 04/07/2025
- Location
- Chandler, AZ, United States
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 6
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.
Product Description
Molding Equipment. WCM series. Model WCM-330GL-i
Distribution Pattern
US
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.