Class II
Medical Device Recall: Molding Equipment. WCM series. Model WCM-330GL-i
Apic Yamada America · April 7, 2025
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.
Distribution
US
Quantity Affected
6
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2150-2025
Status: ongoing
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