Electrolux Home Products Inc.

Complete recall history across all FDA and CPSC categories — 6 total recalls

Electrolux Home Products Inc. 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 (6)

CPSC consumer product recalls by Electrolux Home Products Inc.

Date Product Hazard
May 16, 2024 Frigidaire and Kenmore Smooth-top Freestanding Electric Ranges Depending on the model, the surface heating elements can: 1) turn on spontaneously without being ...
Aug 31, 2023 Frigidaire Stainless-Steel 30-inch 4 Burner and 36-inch 5 Burner Gas Cooktops Plastic control knobs with a black shaft on the cooktop can crack or break during use, posing a r...
Oct 20, 2010 Frigidaire and Electrolux ICON Smoothtop Electric Cooktops and Frigidaire Sli... Liquids can pool under the control knob and cause the surface heating element to turn on unexpect...
Nov 23, 2009 Electrolux ICON and Kenmore Pro 30" Gas Ranges An incorrect part allows more fuel to pass to the range's oven than can be burned efficiently, ca...
Dec 5, 2004 Husqvarna Lawn Tractors, models LTH18542A and LTH18542B These lawn tractors can develop abrasions on the fuel tank because of the fuel line clamp's locat...
Jun 2, 2004 Room Air Conditioning and Heating Units The heating coil in the units can be damaged during assembly, causing an electrical short and ove...

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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