Recall Z-2150-2025— Apic Yamada America

Name: FDA recall Z-2150-2025
Creator: U.S. Food and Drug Administration
Published: 2025-04-07

Class II · Ongoing

Class II FDA medical device recall by Apic Yamada America, initiated 2025-04-07. FDA's recall record names no specific 510(k) clearance for this event. Product: Molding Equipment. WCM series. Model WCM-330GL-i. Reason: 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..

Recalling firm: Apic Yamada America
Classification: Class II
Status: Ongoing
Initiated: 2025-04-07
Firm location: Chandler, AZ, United States

Product description

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

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.