Cybex International
Complete recall history across all FDA and CPSC categories, 5 total recalls
Cybex International 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 Cybex International
| Date | Product | Hazard |
|---|---|---|
| May 10, 2016 | Decline free weight benches | The frame on the bench can collapse forward onto the user, posing an impact injury hazard. |
| Aug 25, 2015 | Arm Curl Machines | The swivel handles can break off from the frame causing users to hit themselves in the face or he... |
| Jan 9, 2014 | Olympic Decline free weight bench | The frame of the bench can collapse forward onto the user, posing fall and injury hazards. |
| Oct 22, 2007 | Cybex or Trotter Treadmills | During repairs associated with the October 8, 2003 recall, wire nuts were installed improperly, c... |
| Oct 7, 2003 | Cybex or Trotter Treadmill | Fire hazard because of overheating and ignition of dust inside the treadmill's hood. The dust acc... |
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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