Yamaha Motor Corporation
Complete recall history across all FDA and CPSC categories — 6 total recalls
Recall Summary
Yamaha Motor Corporation appears in recall records across 2 categories. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (2)
FDA medical device enforcement actions by Yamaha Motor Corporation
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 17, 2024 | Yamaha Surface Mounter YR series, YS series, i-Pulse series, Sigma series, S ... | Non-medical laser products which were determined to not be in compliance with... | Class II |
| Apr 17, 2024 | Optical Inspection System, YSi series, YRi series. Affected models: YSi-V, YS... | Non-medical laser products which were determined to not be in compliance with... | Class II |
Product Recalls (4)
CPSC consumer product recalls by Yamaha Motor Corporation
| Date | Product | Hazard |
|---|---|---|
| Jun 30, 2015 | Yamaha SRViper snowmobiles | The brake line and its components can come in contact with the clutch causing the brakes to fail,... |
| Apr 14, 2015 | Yamaha Viking VI | The rear wheels can loosen and cause the rear end of the vehicle to wobble or the rear wheels to ... |
| Apr 12, 2005 | Yamaha Raptor YFM660R ATVs | In February 2004, Yamaha announced a voluntary recall of Raptor YFM660R ATVs. Vibration from the ... |
| Apr 12, 2005 | Yamaha PW80 and TT-R90 Off-Road Motorcycles and Grizzly 125 ATVs | In September 2004, Yamaha announced a voluntary recall of PW80 and TTR90 Off-Road Motorcycles and... |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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