Recall archive / FDA device enforcement
Molding Equipment. WCM series. Model WCM-330GL-i — FDA record Z-2150-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Apr 7, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class II
- Recalling firm
- Apic Yamada America
- Quantity
- 6
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2150-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | None. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Aug 6, 2025
- Recall initiation date
- Apr 7, 2025
- Center classification date
- Jul 31, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.