Robert Bosch Tool Corp.

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

Robert Bosch Tool Corp. 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 Robert Bosch Tool Corp.

Date Product Hazard
Aug 14, 2007 SkilĀ® brand Circular Saws The trigger switch on the circular saw can be locked on or the switch can be turned on without th...
Jun 8, 2006 Vermont AmericanĀ® Abrasive Cut-Off Wheels The Abrasive Cut-Off Wheel packages are not properly labeled with precautionary information on pr...
Jun 8, 2006 Vermont AmericanĀ® 13-inch-Long Masonry Drill Bits The drill bit packages are not properly labeled with precautionary information on proper use and ...
May 17, 2005 BOSCH Circular Saws The lower blade guard can malfunction, creating a risk of injury as severe as amputation.
Nov 14, 2004 Type 1 Abrasive Cut-Off Wheels These abrasive cut-off wheels do not have correct speed rating labels. If used at the labeled spe...

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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