Severity
Moderate
Magnum and Matrix Fitness Multi-Station Strength Training Towers Recalled by Johnson Health Tech Due to Injury Hazard
Reported: April 25, 2014 Initiated: April 25, 2014 #14160 About 1,100 strength training towers units
Johnson Health Tech North America, Inc. of Cottage Grove, Wis. issued this CPSC recall on April 25, 2014. Classified as Moderate severity. Approximately About 1,100 strength training towers units are affected. The recall was issued because: The plastic connectors that link the strength training stations' towers can slide out or break, posing an injury hazard…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
Recall Insight
This CPSC action (record #14160) was formally reported on April 25, 2014. It is classified under Moderate severity, with a current status of Active. Johnson Health Tech North America, Inc. of Cottage Grove, Wis. is listed as the recalling firm. Federal records indicate About 1,100 strength training towers units are affected.
The documented reason for this recall is: The plastic connectors that link the strength training stations' towers can slide out or break, posing an injury hazard to consumers. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Owners should immediately prevent people from using the multi-station strength training towers and contact Johnson Health Tech North America to schedule a free repair. — consumers holding this product should act on that instruction rather than relying on general guidance.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 12 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Recall Distribution by Severity Class
Units Affected
About 1,100 strength training towers
Related Recalls
6
6 from same agency
Product Description
This recall involves all Magnum and Matrix Fitness 900 Pro Series multi-station strength training towers used at commercial fitness facilities such as health clubs, hotels, apartment complexes and rehabilitation centers; schools and municipal facilities. The machines involved in this recall were sold in various multi-station configurations. The machines include, but are not limited to, the adjustable pulley, the dual adjustable pulley, the triceps push down and the bicep/tricep pull down. Magnum or Matrix appear on the serial number label at the base of each unit.
Reason for Recall
The plastic connectors that link the strength training stations' towers can slide out or break, posing an injury hazard to consumers.
Remedy
Owners should immediately prevent people from using the multi-station strength training towers and contact Johnson Health Tech North America to schedule a free repair.
Details
- Units Affected
- About 1,100 strength training towers
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 14160 |
| Date reported | April 25, 2014 |
| Date initiated | April 25, 2014 |
| Recalling firm | Johnson Health Tech North America, Inc. of Cottage Grove, Wis. |
| Units affected | About 1,100 strength training towers |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
Frequently Asked Questions
What product was recalled? ▼
This recall involves all Magnum and Matrix Fitness 900 Pro Series multi-station strength training towers used at commercial fitness facilities such as health clubs, hotels, apartment complexes and rehabilitation centers; schools and municipal facilities. The machines involved in this recall were sold in various multi-station configurations. The machines include, but are not limited to, the adjustable pulley, the dual adjustable pulley, the triceps push down and the bicep/tricep pull down. Magnum or Matrix appear on the serial number label at the base of each unit.. Recalled by Johnson Health Tech North America, Inc. of Cottage Grove, Wis.. Units affected: About 1,100 strength training towers.
Why was this product recalled? ▼
The plastic connectors that link the strength training stations' towers can slide out or break, posing an injury hazard to consumers.
What should consumers do? ▼
Owners should immediately prevent people from using the multi-station strength training towers and contact Johnson Health Tech North America to schedule a free repair.
Which agency issued this recall? ▼
This recall was issued by the CPSC on April 25, 2014. Severity: Moderate. Recall number: 14160.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (14160) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
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Recall Context
Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
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Data Sources
Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
- Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- U.S. Census Bureau ACS — demographic + housing + income data. census.gov/programs-surveys/acs
- BLS Occupational Employment and Wage Statistics (OEWS) — wage + employment by occupation. bls.gov/oes
- BEA Regional Economic Accounts — GDP + personal income by state/metro. bea.gov/data/regional
- U.S. Census Bureau County Business Patterns — establishment + employment by industry. census.gov/cbp
- IRS Statistics of Income (SOI) — tax-return aggregate data. irs.gov/statistics
- data.gov — U.S. federal open-data portal — discovery layer for additional federal sources. data.gov
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).