FDA Device recall Z-2150-2025
Molding Equipment
- FDA Device
- Class II
- ongoing
- Published 2025-08-06
On 2025-08-06 the FDA classified a Class II recall of Molding Equipment by Apic Yamada America, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2150-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-04-07 |
| Published | 2025-08-06 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Apic Yamada America |
| Distribution | n/a |
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.
Identifiers
| code_info | None. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2150-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.