FDA recall Z-2150-2025

Apic Yamada America · Class II · device

Product

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.

Distribution

Key facts

Status: Ongoing
Initiation date: 2025-04-07
Report date: 2025-08-06
Voluntary/Mandated: FDA Mandated
Location: Chandler, AZ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2150-2025