# FDA recall Z-1815-2024

> **YAMAHA MOTOR CORPORATION** · Class II · device recall initiated 2024-04-17.

## 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

## Reason for recall

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.

## Distribution

US Nationwide

## Key facts

- **Recall number:** Z-1815-2024
- **Recalling firm:** YAMAHA MOTOR CORPORATION
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-17
- **Report date:** 2024-05-29

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Marietta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1815-2024

## Citation

> AI Analytics. FDA recall Z-1815-2024. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1815-2024. Source: US FDA. Licensed CC0.

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