Class II — YAMAHA MOTOR CORPORATION
| Recalling firm | YAMAHA MOTOR CO LTD |
|---|---|
| Registered facility | YAMAHA MOTOR CO LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Non-medical laser products which were determined to not be in compliance with 21 C.F.R. 1010.2 in that they currently do not bear the required certification label. |
| Product | Yamaha Surface Mounter YR series, YS series, i-Pulse series, Sigma series, S series, M series. Affected models: YSM10, YSM20R(SV)-1, YSM20R(SV)-2, YSM20R-1, YSM20R-2, YSM20-1, YSM20-2, YSM20W-2, YRM20-1, YRM20-2, SIGMA-G5S2, S20, M20 ***Updated as of 6/10/2024*** Surface Mounter model S10, YC8. Component Dispenser model YSD |
| Quantity | 376 |
| Distribution | US Nationwide |
| Initiated | 2024-04-17 |
| Classified | 2024-05-20 |
| Recall number | Z-1815-2024 |
| Initiation | FDA Mandated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — YAMAHA MOTOR CORPORATION (Z-1815-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94590/
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