The Toro Company

Complete recall history across all FDA and CPSC categories — 5 total recalls

The Toro Company appears in recall records across 1 category. 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.

Product Recalls (5)

CPSC consumer product recalls by The Toro Company

Date Product Hazard
Feb 17, 2021 Toro Power Max Snowthrowers The auger can fail to disengage when the control lever is released, posing an amputation hazard.
Apr 25, 2011 Toro Power Clear Snowblower and the Toro 20" Recycler Mower The carburetors on both products develop fuel leaks and can ignite when exposed to an ignition so...
Jul 13, 2010 Power Clear 180 Single Stage Snow Blowers Exposure to ethanol in gasoline can cause the carburetor needle to become corroded. A corroded ne...
Jul 25, 2007 Toro Power Sweep Electric Blowers The blower's impeller, which is a rotating component on the blower, can break, resulting in piece...
Aug 2, 2006 Toro Snow Commander and CCR Single Stage Snowthrowers The plastic fuel tank can crack and leak gasoline, posing a risk of fire and injury.

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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