Black & Decker (U.S.) Inc.
Complete recall history across all FDA and CPSC categories, 6 total recalls
Black & Decker (U.S.) 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 Black & Decker (U.S.) Inc.
| Date | Product | Hazard |
|---|---|---|
| Sep 28, 2010 | Black & Decker and Craftsman brand cordless electric lawnmowers | The lawnmower's motor and blade can unexpectedly turn on after the mower's safety key is removed,... |
| Sep 8, 2010 | Black & Decker Random Orbit Sanders | The black plastic disc (called the platen) that holds the sandpaper can fly off or break apart du... |
| Aug 3, 2009 | Black & Decker GH1000 Grasshog XP String Trimmer/Edgers | The trimmer/edger's spool, spool cap and pieces of trimmer string can come loose during use and b... |
| Jul 19, 2007 | Black & Decker GH1000 Grasshog XP String Trimmer/Edgers | The trimmer/edger's spool, spool cap and pieces of trimmer string can come loose during use and b... |
| Oct 9, 2006 | Black & Decker BV4000 Type 1 Blower/Vacs | A loose connection between the blower/vac and an extension cord can cause overheating, posing a f... |
| Aug 15, 2006 | Black & Decker and Craftsman Brand Cordless Electric Lawnmowers | An electrical component in the lawnmowers can overheat, posing a fire hazard. |
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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