Bassett Furniture Industries
Complete recall history across all FDA and CPSC categories — 5 total recalls
Bassett Furniture Industries 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 Bassett Furniture Industries
| Date | Product | Hazard |
|---|---|---|
| Nov 21, 2010 | Bassettbaby drop-side cribs with external plastic hardware | The cribs' drop-side rail can malfunction, detach or otherwise fail, causing part of the drop sid... |
| Feb 1, 1984 | Candlelite and Mandalay cribs | A crib that has been the subject of an intensive recall effort since 1978 was involved in two add... |
| Feb 13, 1980 | "Mandalay" and "Candlelite" style cribs | The U.S. Consumer Product Safety Commission provisionally has accepted a consent agreement with B... |
| Nov 27, 1979 | "Mandalay" and "Candlelite" style cribs | The Bassett cribs requiring modification include the "Mandalay" and "Candlelite" style beds. They... |
| May 4, 1978 | Bassett cribs with model numbers 5126, 5621 and 5225 | The Commission believes that the design of the headboards and footboards in Bassett cribs with mo... |
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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