DEWALT Industrial Tool Co.

Complete recall history across all FDA and CPSC categories — 7 total recalls

DEWALT Industrial Tool Co. 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 (7)

CPSC consumer product recalls by DEWALT Industrial Tool Co.

Date Product Hazard
Apr 28, 2008 DEWALT DW744 Jobsite Table Saws The pivot bracket on the saw can separate which can misalign the blade and the fence and cause ki...
Jan 3, 2007 DEWALT DG2900 Portable Generators A ground fault circuit interrupter (GFCI) installed on the generator could fail to operate proper...
Dec 20, 2006 DEWALT Model DW660 Cut-Out Tools The cord wire in these units could be damaged internally, posing a shock hazard to consumers.
Dec 20, 2006 DEWALT DC305 Model Reciprocating Saws The switch on these saws can short circuit, posing a fire hazard.
Nov 7, 2006 DeWalt DW378G/DW378GT Framing Saws and DC300 Circular Saws The lower blade guard can fail to close, leaving the blade exposed and presenting a laceration ha...
Jun 2, 2005 DeWALT Framing Nailers (model numbers listed below) The contact trip on some of the nailers could malfunction and cause a nail to eject unexpectedly,...
Nov 24, 1998 DeWalt framing saws The saw's lower blade guard can fail to fully close during use, leaving the blade exposed and pre...

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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